TopoSNP

NECTAR

Disease-related non-synonymous mutations

VarySysDB

Various types of human gene polymorphism

rVarbase

Annotated SNPs within regulatory DNA elements

HGVS Databases

A compilation of human mutation databases

dbPSHP

A database of recent positive selection across human populations

dbSAP

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

GWAS Diagram Browser

SNPlogic

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

VADE

VarySysDB Disease Edition: Disease-associated genomic polymorphisms

1000 Genomes Selection Browser

Signature of selection in the human genomes

Cypriot national mutation database

Disease mutations in the Cypriot population

TPMD - Taiwan polymorphic microsatellite marker database

Microsatellite markers genotyped in Taiwanese populations

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 ...

Integrated Genomic Database of Non-Small Cell Lung Cancer

Integrated Genomic Database of Non-Small Cell Lung Cancer.

PolyDoms

An integrated database of human coding single nucleotide polymorphisms (SNPs) and their annotations.

BodyParts3D

Database of human anatomy, represented as 3D anatomical concepts

Patrocles

Polymorphic miRNA-mediated gene regulation in vertebrates

HaploReg

HaploReg is a tool for exploring annotations of the noncoding genome at variants on haplotype blocks, such as candidate regulatory SNPs at disease-associated loci. Using LD information from the 1000 G ...

InvFEST

Polymorphic inversions in the human genome