FAIRsharing.dvwz21; Last edited: July 7, 2021, 8:36 a.m.; Last accessed: Jan 03 2022 7:07 p.m.

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:26.634110

gwasdb
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:26.634110

Other names: gwasdb

This source may no longer be available. No known URL could be resolved successfully.

GWASdb comprises of collections of traits/diseases associated SNP (TASs) from current GWAS and their comprehensive functional annotations, as well as disease classifications.

Webpage:

http://jjwanglab.org/gwasdb

Publications:

Publications
More detailed information about this field from each metasource.

GWASdb: a database for human genetic variants identified by genome-wide association studies
PMID: 22139925
metasource: Fairsharing.org
version: FAIRsharing.org: GWASdb; GWASdb; DOI: https://doi.org/10.25504/FAIRsharing.dvwz21; Last edited: July 7, 2021, 8:36 a.m.; Last accessed: Jan 03 2022 7:07 p.m.

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:26.634110

GWASdb v2: an update database for human genetic variants identified by genome-wide association studies
PMID: 26615194
metasource: Fairsharing.org
version: FAIRsharing.org: GWASdb; GWASdb; DOI: https://doi.org/10.25504/FAIRsharing.dvwz21; Last edited: July 7, 2021, 8:36 a.m.; Last accessed: Jan 03 2022 7:07 p.m.

Genetic variant representation, annotation and prioritization in the post-GWAS era
PMID: 22801476
metasource: Fairsharing.org
version: FAIRsharing.org: GWASdb; GWASdb; DOI: https://doi.org/10.25504/FAIRsharing.dvwz21; Last edited: July 7, 2021, 8:36 a.m.; Last accessed: Jan 03 2022 7:07 p.m.

http://dx.doi.org/10.1093/nar/GKR1182
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

GWASdb: a database for human genetic variants identified by genome-wide association studies PubMed citations: 101.

101 articles citing: GWASdb: a database for human genetic variants identified by genome-wide association studies

DisPhaseDB: An integrative database of diseases related variations in liquid-liquid phase separation proteins. PMID:35685370
Stimulation of the hepatoportal nerve plexus with focused ultrasound restores glucose homoeostasis in diabetic mice, rats and swine. PMID:35361935
Dysregulation of Human Somatic piRNA Expression in Parkinson's Disease Subtypes and Stages. PMID:35269612
Cis-regulated expression of non-conserved lincRNAs associates with cardiometabolic related traits. PMID:35017681
Resolvin E1-ChemR23 Axis Regulates the Hepatic Metabolic and Inflammatory Transcriptional Landscape in Obesity at the Whole Genome and Exon Level. PMID:35004828
ELMO1 signaling is a promoter of osteoclast function and bone loss. PMID:34404802
Impaired Right Ventricular Calcium Cycling Is an Early Risk Factor in R14del-Phospholamban Arrhythmias. PMID:34204946
Non-coding Single Nucleotide Variants of Renin and the (Pro)renin Receptor are Associated with Polygenic Diseases in a Bangladeshi Population. PMID:33677630
Coordinated control of adiposity and growth by anti-anabolic kinase ERK7. PMID:33369866
DNA Methylation Patterns of Chronic Explosive Breaching in U.S. Military Warfighters. PMID:33192958
Incorporating prior knowledge into regularized regression. PMID:32915960
Premature Activation of Immune Transcription Programs in Autoimmune-Predisposed Mouse Embryonic Stem Cells and Blastocysts. PMID:32796510
A single genetic locus associated with pediatric fractures: A genome-wide association study on 3,230 patients. PMID:32742401
Shared genetic etiology underlying late-onset Alzheimer's disease and posttraumatic stress syndrome. PMID:32588970
pyMeSHSim: an integrative python package for biomedical named entity recognition, normalization, and comparison of MeSH terms. PMID:32552728
Genome-Wide Analysis Identifies NURR1-Controlled Network of New Synapse Formation and Cell Cycle Arrest in Human Neural Stem Cells. PMID:32522891
PS4DR: a multimodal workflow for identification and prioritization of drugs based on pathway signatures. PMID:32503412
Diversity of RNA-Binding Proteins Modulating Post-Transcriptional Regulation of Protein Expression in the Maturing Mammalian Oocyte. PMID:32182827
The unique expression profile of FAM19A1 in the mouse brain and its association with hyperactivity, long-term memory and fear acquisition. PMID:32123192
GWAS Atlas: a curated resource of genome-wide variant-trait associations in plants and animals. PMID:31566222
Integrative transcriptome imputation reveals tissue-specific and shared biological mechanisms mediating susceptibility to complex traits. PMID:31444360
HPO-Shuffle: an associated gene prioritization strategy and its application in drug repurposing for the treatment of canine epilepsy. PMID:31427480
Genome-wide analysis indicates association between heterozygote advantage and healthy aging in humans. PMID:31266448
Pathway-specific protein domains are predictive for human diseases. PMID:31075101
Improved annotation of the domestic pig genome through integration of Iso-Seq and RNA-seq data. PMID:31064321
Analysis of Topological Parameters of Complex Disease Genes Reveals the Importance of Location in a Biomolecular Network. PMID:30769902
Trinucleotide Base Pair Stacking Free Energy for Understanding TF-DNA Recognition and the Functions of SNPs. PMID:30713839
A noncanonical role for the engulfment gene ELMO1 in neutrophils that promotes inflammatory arthritis. PMID:30643265
Identification of LncRNA Linc00513 Containing Lupus-Associated Genetic Variants as a Novel Regulator of Interferon Signaling Pathway. PMID:30619325
Coevolving residues inform protein dynamics profiles and disease susceptibility of nSNVs. PMID:30496278
AnimalTFDB 3.0: a comprehensive resource for annotation and prediction of animal transcription factors. PMID:30204897
A Genome-Wide Association Study of α-Synuclein Levels in Cerebrospinal Fluid. PMID:29959729
Linkage mapping of yeast cross protection connects gene expression variation to a higher-order organismal trait. PMID:29649251
Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human disease. PMID:29494619
Formalising recall by genotype as an efficient approach to detailed phenotyping and causal inference. PMID:29459775
The Porphyromonas gingivalis/Host Interactome Shows Enrichment in GWASdb Genes Related to Alzheimer's Disease, Diabetes and Cardiovascular Diseases. PMID:29311898
Context-dependent compensation among phosphatidylserine-recognition receptors. PMID:29116131
Dysregulation of Cortical Neuron DNA Methylation Profile in Autism Spectrum Disorder. PMID:29028941
Analytical Strategy to Prioritize Alzheimer's Disease Candidate Genes in Gene Regulatory Networks Using Public Expression Data. PMID:28800327
Using the Neandertal genome to study the evolution of small insertions and deletions in modern humans. PMID:28778150
Exploring genetic associations with ceRNA regulation in the human genome. PMID:28472449
Long noncoding RNA LINC00305 promotes inflammation by activating the AHRR-NF-κB pathway in human monocytes. PMID:28393844
Functional implications of Neandertal introgression in modern humans. PMID:28366169
The interactome of the copper transporter ATP7A belongs to a network of neurodevelopmental and neurodegeneration factors. PMID:28355134
Systematic analyses of drugs and disease indications in RepurposeDB reveal pharmacological, biological and epidemiological factors influencing drug repositioning. PMID:28200013
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. PMID:27876822
SZGR 2.0: a one-stop shop of schizophrenia candidate genes. PMID:27733502
Data sources for in vivo molecular profiling of human phenotypes. PMID:27599755
eSNPO: An eQTL-based SNP Ontology and SNP functional enrichment analysis platform. PMID:27470167
The harmonizome: a collection of processed datasets gathered to serve and mine knowledge about genes and proteins. PMID:27374120
5-Hydroxymethylcytosine Remodeling Precedes Lineage Specification during Differentiation of Human CD4(+) T Cells. PMID:27346350
Explaining the disease phenotype of intergenic SNP through predicted long range regulation. PMID:27280978
Rising Strengths Hong Kong SAR in Bioinformatics. PMID:26961385
Introns: The Functional Benefits of Introns in Genomes. PMID:26865841
Epigenome overlap measure (EPOM) for comparing tissue/cell types based on chromatin states. PMID:26817822
Primary Immunodeficiencies and Inflammatory Disease: A Growing Genetic Intersection. PMID:26791050
Introgression of Neandertal- and Denisovan-like Haplotypes Contributes to Adaptive Variation in Human Toll-like Receptors. PMID:26748514
Forward Individualized Medicine from Personal Genomes to Interactomes. PMID:26696898
Testing for Ancient Selection Using Cross-population Allele Frequency Differentiation. PMID:26596347
SEA: a super-enhancer archive. PMID:26578594
Discover hidden splicing variations by mapping personal transcriptomes to personal genomes. PMID:26578562
Human genotype-phenotype databases: aims, challenges and opportunities. PMID:26553330
Polymorphisms involving gain or loss of CpG sites are significantly enriched in trait-associated SNPs. PMID:26503467
Methods for biological data integration: perspectives and challenges. PMID:26490630
Integrative analysis of human protein, function and disease networks. PMID:26399914
Endocannabinoid signalling in reward and addiction. PMID:26373473
Translational genomics for plant breeding with the genome sequence explosion. PMID:26269219
The Use of Non-Variant Sites to Improve the Clinical Assessment of Whole-Genome Sequence Data. PMID:26147798
The support of human genetic evidence for approved drug indications. PMID:26121088
The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease. PMID:26119816
Publisher’s Note:Abstraction for data integration:Fusing mammalian molecular, cellular and phenotype big datasets for better knowledge extraction. PMID:26101093
Re-annotation of presumed noncoding disease/trait-associated genetic variants by integrative analyses. PMID:25819875
Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions. PMID:25807536
Biological databases for human research. PMID:25712261
Deciphering Genome Environment Wide Interactions Using Exposed Subjects Only. PMID:25694100
In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk loci. PMID:25552398
Systematic analysis of the in situ crosstalk of tyrosine modifications reveals no additional natural selection on multiply modified residues. PMID:25476580
VaDE: a manually curated database of reproducible associations between various traits and human genomic polymorphisms. PMID:25361969
VAS: a convenient web portal for efficient integration of genomic features with millions of genetic variants. PMID:25306238
On the identification of potential regulatory variants within genome wide association candidate SNP sets. PMID:24920305
Improving the accuracy of whole genome prediction for complex traits using the results of genome wide association studies. PMID:24663104
Unifying immunology with informatics and multiscale biology. PMID:24448569
OGA: an ontological tool of human phenotypes with genetic associations. PMID:24308566
CNVannotator: a comprehensive annotation server for copy number variation in the human genome. PMID:24244640
Detection of regulatory SNPs in human genome using ChIP-seq ENCODE data. PMID:24205329
dbPSHP: a database of recent positive selection across human populations. PMID:24194603
RAvariome: a genetic risk variants database for rheumatoid arthritis based on assessment of reproducibility between or within human populations. PMID:24158836
SIDD: a semantically integrated database towards a global view of human disease. PMID:24146757
Understanding human variation in infectious disease susceptibility through clinical and cellular GWAS. PMID:23935492
DNA methylation contributes to natural human variation. PMID:23908385
dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations. PMID:23843252
GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications. PMID:23723249
Prioritization of genetic variants in the microRNA regulome as functional candidates in genome-wide association studies. PMID:23595788
Needles in the genetic haystack of lipid disorders: single nucleotide polymorphisms in the microRNA regulome. PMID:23505316
Neurocarta: aggregating and sharing disease-gene relations for the neurosciences. PMID:23442263
RNAsnp: efficient detection of local RNA secondary structure changes induced by SNPs. PMID:23315997
Semantically enabling a genome-wide association study database. PMID:23244533
The 2013 Nucleic Acids Research Database Issue and the online molecular biology database collection. PMID:23203983
H2DB: a heritability database across multiple species by annotating trait-associated genomic loci. PMID:23193255
Genetic variant representation, annotation and prioritization in the post-GWAS era. PMID:22801476
A functional single-nucleotide polymorphism in the promoter of the gene encoding interleukin 6 is associated with susceptibility to tuberculosis. PMID:22457277
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies PubMed citations: 93.

93 articles citing: GWASdb v2: an update database for human genetic variants identified by genome-wide association studies

mGWAS-Explorer: Linking SNPs, Genes, Metabolites, and Diseases for Functional Insights. PMID:35736459
Somatic point mutations are enriched in non-coding RNAs with possible regulatory function in breast cancer. PMID:35672401
Machine learning methods applied to genotyping data capture interactions between single nucleotide variants in late onset Alzheimer's disease. PMID:35415203
FGF21 modulates mitochondrial stress response in cardiomyocytes only under mild mitochondrial dysfunction. PMID:35385313
Diseases 2.0: a weekly updated database of disease-gene associations from text mining and data integration. PMID:35348648
CATA: a comprehensive chromatin accessibility database for cancer. PMID:35134148
LncRNA functional annotation with improved false discovery rate achieved by disease associations. PMID:35035785
Facilitating Antiviral Drug Discovery Using Genetic and Evolutionary Knowledge. PMID:34834924
CircleBase: an integrated resource and analysis platform for human eccDNAs. PMID:34792166
TcoFBase: a comprehensive database for decoding the regulatory transcription co-factors in human and mouse. PMID:34718747
Recent innovations and in-depth aspects of post-genome wide association study (Post-GWAS) to understand the genetic basis of complex phenotypes. PMID:34689168
webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study. PMID:34669946
Repurposing new drug candidates and identifying crucial molecules underlying PCOS Pathogenesis Based On Bioinformatics Analysis. PMID:34480296
Seeing the forest through the trees: prioritising potentially functional interactions from Hi-C. PMID:34454581
Biomolecule and Bioentity Interaction Databases in Systems Biology: A Comprehensive Review. PMID:34439912
The Causal Relationship Between Body Mass Index and the Risk of Osteoarthritis. PMID:34103976
Enhancer release and retargeting activates disease-susceptibility genes. PMID:34040254
Prediction of Synergistic Drug Combinations for Prostate Cancer by Transcriptomic and Network Characteristics. PMID:33986671
Novel lincRNA Discovery and Tissue-Specific Gene Expression across 30 Normal Human Tissues. PMID:33919168
SNPs in genes encoding for IL-10, TNF-α, and NFκB p105/p50 are associated with clinical prognostic factors for patients with Hodgkin lymphoma. PMID:33684151
Coupling of autism genes to tissue-wide expression and dysfunction of synapse, calcium signalling and transcriptional regulation. PMID:33338084
LincSNP 3.0: an updated database for linking functional variants to human long non-coding RNAs, circular RNAs and their regulatory elements. PMID:33219661
VARAdb: a comprehensive variation annotation database for human. PMID:33095866
Ultrafast and scalable variant annotation and prioritization with big functional genomics data. PMID:33060171
ABC-GWAS: Functional Annotation of Estrogen Receptor-Positive Breast Cancer Genetic Variants. PMID:32765587
Genome-Wide Analysis Identifies NURR1-Controlled Network of New Synapse Formation and Cell Cycle Arrest in Human Neural Stem Cells. PMID:32522891
PCOSBase: a manually curated database of polycystic ovarian syndrome. PMID:31725861
CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies. PMID:31691819
The DisGeNET knowledge platform for disease genomics: 2019 update. PMID:31680165
GWAS Central: a comprehensive resource for the discovery and comparison of genotype and phenotype data from genome-wide association studies. PMID:31612961
GWAS Atlas: a curated resource of genome-wide variant-trait associations in plants and animals. PMID:31566222
Myopia genetics in genome-wide association and post-genome-wide association study era. PMID:31544047
Evolutionary and functional impact of common polymorphic inversions in the human genome. PMID:31530810
regBase: whole genome base-wise aggregation and functional prediction for human non-coding regulatory variants. PMID:31511901
Integrated Analysis of DNA Methylation and Biochemical/Metabolic Parameter During the Long-Term Isolation Environment. PMID:31402871
Genome-wide analysis indicates association between heterozygote advantage and healthy aging in humans. PMID:31266448
Protein-Protein Interaction Network Analysis Reveals Several Diseases Highly Associated with Polycystic Ovarian Syndrome. PMID:31216618
TAGOOS: genome-wide supervised learning of non-coding loci associated to complex phenotypes. PMID:31045203
Risk of cognition alteration and emotional frailty via circulating transcriptome in treatment naïve head and neck squamous cell cancer patients. PMID:30949427
PheWAS-Based Systems Genetics Methods for Anti-Breast Cancer Drug Discovery. PMID:30781719
Pregnancy Epigenetic Signature in T Helper 17 and T Regulatory Cells in Multiple Sclerosis. PMID:30671056
Into the Wild: GWAS Exploration of Non-coding RNAs. PMID:30619888
Identification of LncRNA Linc00513 Containing Lupus-Associated Genetic Variants as a Novel Regulator of Interferon Signaling Pathway. PMID:30619325
Novel disease syndromes unveiled by integrative multiscale network analysis of diseases sharing molecular effectors and comorbidities. PMID:30598089
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources. PMID:30476213
ANCO-GeneDB: annotations and comprehensive analysis of candidate genes for alcohol, nicotine, cocaine and opioid dependence. PMID:30403795
Chromatin accessibility landscape of articular knee cartilage reveals aberrant enhancer regulation in osteoarthritis. PMID:30341348
AGD: Aneurysm Gene Database. PMID:30256987
Loss of LDAH associated with prostate cancer and hearing loss. PMID:30169630
Computational resources associating diseases with genotypes, phenotypes and exposures. PMID:30102366
A revised airway epithelial hierarchy includes CFTR-expressing ionocytes. PMID:30069044
Enabling Precision Cardiology Through Multiscale Biology and Systems Medicine. PMID:30062151
KDM2A/B lysine demethylases and their alternative isoforms in development and disease. PMID:30059280
Network-based approach to prediction and population-based validation of in silico drug repurposing. PMID:30002366
Prioritization and functional assessment of noncoding variants associated with complex diseases. PMID:29996888
Systems Analyses Reveal Physiological Roles and Genetic Regulators of Liver Lipid Species. PMID:29909277
Genetic Regulation of Plasma Lipid Species and Their Association with Metabolic Phenotypes. PMID:29909275
Exon Array Biomarkers for the Differential Diagnosis of Schizophrenia and Bipolar Disorder. PMID:29888231
The MR-Base platform supports systematic causal inference across the human phenome. PMID:29846171
GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits. PMID:29771388
Post genome-wide association analysis: dissecting computational pathway/network-based approaches. PMID:29701762
The SNPcurator: literature mining of enriched SNP-disease associations. PMID:29688369
Mammalian genomic regulatory regions predicted by utilizing human genomics, transcriptomics, and epigenetics data. PMID:29618048
Facilitating Anti-Cancer Combinatorial Drug Discovery by Targeting Epistatic Disease Genes. PMID:29570606
Global analysis of A-to-I RNA editing reveals association with common disease variants. PMID:29527417
Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. PMID:29274321
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus. PMID:29142228
NONCODEV5: a comprehensive annotation database for long non-coding RNAs. PMID:29140524
PedAM: a database for Pediatric Disease Annotation and Medicine. PMID:29126123
eRAM: encyclopedia of rare disease annotations for precision medicine. PMID:29106618
Concise Review: Epigenetic Regulation of Hematopoiesis: Biological Insights and Therapeutic Applications. PMID:29080249
HEDD: Human Enhancer Disease Database. PMID:29077884
Chronic obstructive pulmonary disease candidate gene prioritization based on metabolic networks and functional information. PMID:28873096
Long noncoding RNA LINC00305 promotes inflammation by activating the AHRR-NF-κB pathway in human monocytes. PMID:28393844
The landscape of genetic susceptibility correlations among diseases and traits. PMID:28371808
cepip: context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genes. PMID:28302177
On the relationships in rhesus macaques between chronic ethanol consumption and the brain transcriptome. PMID:28247455
An atlas of human long non-coding RNAs with accurate 5' ends. PMID:28241135
Systematic analyses of drugs and disease indications in RepurposeDB reveal pharmacological, biological and epidemiological factors influencing drug repositioning. PMID:28200013
InterVar: Clinical Interpretation of Genetic Variants by the 2015 ACMG-AMP Guidelines. PMID:28132688
Alternative intronic promoters in development and disease. PMID:28078440
POSTAR: a platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins. PMID:28053162
Comparative analysis of DNA methylome and transcriptome of skeletal muscle in lean-, obese-, and mini-type pigs. PMID:28045116
LincSNP 2.0: an updated database for linking disease-associated SNPs to human long non-coding RNAs and their TFBSs. PMID:27924020
Function-driven discovery of disease genes in zebrafish using an integrated genomics big data resource. PMID:27903883
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). PMID:27899670
The Human Phenotype Ontology in 2017. PMID:27899602
Archaic Hominin Admixture Facilitated Adaptation to Out-of-Africa Environments. PMID:27839976
SZGR 2.0: a one-stop shop of schizophrenia candidate genes. PMID:27733502
COEXPEDIA: exploring biomedical hypotheses via co-expressions associated with medical subject headings (MeSH). PMID:27679477
eSNPO: An eQTL-based SNP Ontology and SNP functional enrichment analysis platform. PMID:27470167
Predicting regulatory variants with composite statistic. PMID:27273672
LBH Gene Transcription Regulation by the Interplay of an Enhancer Risk Allele and DNA Methylation in Rheumatoid Arthritis. PMID:27159840
Genetic variant representation, annotation and prioritization in the post-GWAS era PubMed citations: 18.

18 articles citing: Genetic variant representation, annotation and prioritization in the post-GWAS era

Novel Genetic Variants of ALG6 and GALNTL4 of the Glycosylation Pathway Predict Cutaneous Melanoma-Specific Survival. PMID:31991610
The variome concept: focus on CNVariome. PMID:31890032
HPOAnnotator: improving large-scale prediction of HPO annotations by low-rank approximation with HPO semantic similarities and multiple PPI networks. PMID:31865916
PheGWAS: a new dimension to visualize GWAS across multiple phenotypes. PMID:31860083
Novel genetic variants in HDAC2 and PPARGC1A of the CREB-binding protein pathway predict survival of non-small-cell lung cancer. PMID:31713888
Principles and methods of in-silico prioritization of non-coding regulatory variants. PMID:29288389
Diversity and inclusion in genomic research: why the uneven progress? PMID:28770442
Long non-coding RNAs as novel players in β cell function and type 1 diabetes. PMID:28738846
mTCTScan: a comprehensive platform for annotation and prioritization of mutations affecting drug sensitivity in cancers. PMID:28482068
Long noncoding RNA LINC00305 promotes inflammation by activating the AHRR-NF-κB pathway in human monocytes. PMID:28393844
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies. PMID:26615194
Association of common variants in the calcium-sensing receptor gene with serum calcium levels in East Asians. PMID:25972035
Association analyses confirm five susceptibility loci for systemic lupus erythematosus in the Han Chinese population. PMID:25890262
New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. PMID:24763700
Detection of regulatory SNPs in human genome using ChIP-seq ENCODE data. PMID:24205329
Inference of gene-phenotype associations via protein-protein interaction and orthology. PMID:24194887
dbPSHP: a database of recent positive selection across human populations. PMID:24194603
GWAS3D: Detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications. PMID:23723249
http://dx.doi.org/10.1093/nar/GKR1182

Tags:

Tags
More detailed information about this field from each metasource.

annotation
metasource: Fairsharing.org
version: FAIRsharing.org: GWASdb; GWASdb; DOI: https://doi.org/10.25504/FAIRsharing.dvwz21; Last edited: July 7, 2021, 8:36 a.m.; Last accessed: Jan 03 2022 7:07 p.m.

computational predictions
metasource: Fairsharing.org
version: FAIRsharing.org: GWASdb; GWASdb; DOI: https://doi.org/10.25504/FAIRsharing.dvwz21; Last edited: July 7, 2021, 8:36 a.m.; Last accessed: Jan 03 2022 7:07 p.m.

disease process modeling
metasource: Fairsharing.org
version: FAIRsharing.org: GWASdb; GWASdb; DOI: https://doi.org/10.25504/FAIRsharing.dvwz21; Last edited: July 7, 2021, 8:36 a.m.; Last accessed: Jan 03 2022 7:07 p.m.

genetic polymorphism
metasource: Fairsharing.org
version: FAIRsharing.org: GWASdb; GWASdb; DOI: https://doi.org/10.25504/FAIRsharing.dvwz21; Last edited: July 7, 2021, 8:36 a.m.; Last accessed: Jan 03 2022 7:07 p.m.

genome-wide association study
metasource: Fairsharing.org
version: FAIRsharing.org: GWASdb; GWASdb; DOI: https://doi.org/10.25504/FAIRsharing.dvwz21; Last edited: July 7, 2021, 8:36 a.m.; Last accessed: Jan 03 2022 7:07 p.m.

micro rna (mirna) target site
metasource: Fairsharing.org
version: FAIRsharing.org: GWASdb; GWASdb; DOI: https://doi.org/10.25504/FAIRsharing.dvwz21; Last edited: July 7, 2021, 8:36 a.m.; Last accessed: Jan 03 2022 7:07 p.m.

splice site
metasource: Fairsharing.org
version: FAIRsharing.org: GWASdb; GWASdb; DOI: https://doi.org/10.25504/FAIRsharing.dvwz21; Last edited: July 7, 2021, 8:36 a.m.; Last accessed: Jan 03 2022 7:07 p.m.

human genes and diseases
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

gene-, system- or disease-specific databases
metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

gwas study
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:26.634110

pathology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:26.634110

mapping
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:26.634110

molecular interactions, pathways and networks
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:26.634110

functional, regulatory and non-coding rna
metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:26.634110

computational predictions disease process modeling polymorphism genome-wide association study micro rna (mirna) target site splice site human genes and diseases gene-, system- or disease-specific gwas study pathology mapping molecular interactions, pathways and networks functional, regulatory and non-coding rna

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GWAS Central

Genome-Wide Association Studies Catalog

GWAS Atlas

dbPSHP

Human Ancestry Ontology

Ontology for Genetic Disease Investigations

DistiLD Database: Diseases and Traits in Linkage Disequilibrium Blocks

Type 2 Diabetes Knowledge Portal

G2Cdb

CAUSALdb

PGDB

PubAngioGen

PheWAS

HbVar

SZGR

PCOSKB

IL2Rgbase

DISEASES

Idiopathic Pulmonary Fibrosis (IPF) Genome-wide Association Study

DDMGD