Search
Product
About us
Contact
Blog

GeneSNPs

Names
More detailed information about this field from each metasource.

GeneSNPs
metasource: bio.tools
version: extracted_at: 2022-11-04T11:36:16.433997

genesnps
metasource: bio.tools
version: extracted_at: 2022-11-04T11:36:16.433997

Other names: genesnps

Names

More detailed information about this field from each metasource.

GeneSNPs

metasource: bio.tools
version: extracted_at: 2022-11-04T11:36:16.433997

genesnps

metasource: bio.tools
version: extracted_at: 2022-11-04T11:36:16.433997

Gene-centric map of the genome structure, coding sequences, and identified allelic variation in genes being targeted for a role in disease susceptibility by the NIEHS (National Institute of Evironmental Health Sciences). This database provides a graphical view of all available SNP data including allele frequencies and genotypes in select populations. This information is key in selecting the polymorphic sites needed to examine disease risk in human population studies.

Description

More detailed information about this field from each metasource.

Gene-centric map of the genome structure, coding sequences, and identified allelic variation in genes being targeted for a role in disease susceptibility by the NIEHS (National Institute of Evironmental Health Sciences). This database provides a graphical view of all available SNP data including allele frequencies and genotypes in select populations. This information is key in selecting the polymorphic sites needed to examine disease risk in human population studies.

metasource: bio.tools
version: extracted_at: 2022-11-04T11:36:16.433997

Webpage:

http://www.genome.utah.edu/genesnps/

Webpage

More detailed information about this field from each metasource.

http://www.genome.utah.edu/genesnps/

metasource: bio.tools
version: extracted_at: 2022-11-04T11:36:16.433997

Tags:

Tags
More detailed information about this field from each metasource.

dna polymorphism
metasource: bio.tools
version: extracted_at: 2022-11-04T11:36:16.433997

human biology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:36:16.433997

pathology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:36:16.433997

dna polymorphism human pathology

More to explore:

1/20

Allele Frequency Net Database

The Allele Frequency Net Database (AFND) provides the scientific community with a freely available repository for the storage of frequency data (alleles, genes, haplotypes and genotypes) related to hu ...

HDAM

A resource of human disease associated mutations from next generation sequencing studies.

Allele frequency resource for research and teaching

ALFRED is designed to make allele frequency data on human population samples readily available for use by the scientific and educational communities.

National Institute of Mental Health Data Archive

The National Institute of Mental Health Data Archive (NDA), originally established to support autism research, is an informatics platform and data repository that facilitates data sharing across all o ...

HapMap Project

The SNP Consortium website (http://snp.cshl.org) has undergone many changes since its initial conception three years ago. The database back end has been changed from the venerable ACeDB to the more sc ...

LincSNP

Association of human lncRNAs with disease-related SNPs

Dog Genome SNP Database

Dog Genome SNP Database (DoGSD) is a data container for the variation information of dog/wolf genomes. It was designed and constructed as an SNPs detector and visualization tool to provide the researc ...

Drosophila polymorphism database

Drosophila Polymorphism Database, is a secondary database designed to provide a collection of all the existing polymorphic sequences in the Drosophila genus. It allows, for the first time, the search ...

NextBio gene-centric data

The platform enables biologists to examine a gene, protein, compound or disease of interest in a global, biological, or clinical context.

Adolescent Brain Cognitive Development Data Repository

The ABCD Data Repository houses all data generated by the Adolescent Brain Cognitive Development (ABCD) Study. The ABCD Study is a landmark, longitudinal study of brain development and child health. I ...

al MENA

Middle East and North Africa (MENA) encompass very unique populations, with a rich history and encompasses characteristic ethnic, linguistic and genetic diversity. The genetic diversity of MENA region ...

SCOPe

The ASTRAL compendium provides a set of tools and databases designed to aid investigators in the analysis of protein structure, particularly through the use of sequence comparison. Astral augments SCO ...

Pharmacogenomics Knowledge Base

PharmGKB is a resource that provides information about how human genetic variation affects response to medications. PharmGKB collects, curates and disseminates knowledge about clinically actionable ge ...

NetPath

NetPath is currently one of the largest open-source repository of human signaling pathways that is all set to become a community standard to meet the challenges in functional genomics and systems biol ...

Brassica Genome

This site hosts Brassica genome databases.

OGRe - Organellar Genome Retrieval

OGRe is a relational database containing information on completely sequenced animal mitochondrial genomes. It currently contains 473 species. This is the full set of complete metazoan mitochondrial ge ...

UCSC Genome Browser database

Genome assemblies and aligned annotations for a wide range of vertebrates and model organisms, along with an integrated tool set for visualizing, comparing, analyzing and sharing both publicly availab ...

ORFDB

A major challenge following the sequencing of the human genome is to determine the biological functions of the estimated 30,000 genes. This requires the biochemical characterization of expressed prote ...

Human Phenotype Ontology

The Human Phenotype Ontology (HPO) provides a standardized vocabulary of phenotypic abnormalities encountered in human disease. Each term in the HPO describes a phenotypic abnormality, such as Atrial ...

LncRNADisease

A surprising finding in human transcriptome analysis is that protein-coding sequences only account for a small portion of the genome transcripts (1). The majority of the human genome transcripts are n ...

Previous Next

Need help integrating and/or managing biomedical data?