Cypriot national mutation database

Lowe Syndrome Mutation Database

Mutations in the OCRL1 gene encoding phosphatidylinositol-4,5-bisphosphate 5-phosphatase

HGVS Databases

A compilation of human mutation databases

VarySysDB

Various types of human gene polymorphism

rVarbase

Annotated SNPs within regulatory DNA elements

Alzheimer Disease & Frontotemporal Dementia Mutation Database

The Alzheimer Disease & Frontotemporal Dementia Mutation Database (AD&FTDMDB) aims at collecting all known mutations in the genes related to Alzheimer disease (AD) and fromtotemporal dementias (FTD). ...

GWAS Diagram Browser

dbPSHP

A database of recent positive selection across human populations

dbSAP

Single Amino acid polymorphisms: SNP-derived variation in human proteins

F-SNP

Functional effects of various human SNPs

VADE

VarySysDB Disease Edition: Disease-associated genomic polymorphisms

Parkinson Disease Mutation Database

The Parkinson disease Mutation Database (PDmutDB) aims at collecting all known mutations in the genes related to Parkinson disease (PD). Mutations are collected from the literature and from presentati ...

TopoSNP

Topographic database of non-synonymous SNPs

TPMD - Taiwan polymorphic microsatellite marker database

Microsatellite markers genotyped in Taiwanese populations

1000 Genomes Selection Browser

Signature of selection in the human genomes

Blackfan Anemia mutation database

Blackfan Anemia mutation database.

SNPlogic

Interactive SNP annotation, selection and prioritization system for genotyping projects and/or analysis and interpretation of SNP data.

MDPD

Mutation Database for Parkinson's Disease

HCAD - Human Chromosome Aberration Database

Chromosomal breakpoints and affected genes

Cystic Fibrosis Mutation Database

The Cystic Fibrosis Mutation Database (CFTR1) was initiated by the Cystic Fibrosis Genetic Analysis Consortium in 1989 to increase and facilitate communications among CF researchers, and is maintained ...