The database of Genotype and Phenotype (dbGaP) was developed to archive and distribute the results of studies that have investigated the interaction of genotype and phenotype. Such studies include genome-wide association studies, medical sequencing, molecular diagnostic assays, as well as association between genotype and non-clinical traits.
Browser and portal for NHGRI's ENCODE project. This is the official repository of sequence-related data for the ENCODE Consortium and supports the coordination of data submission, storage, retrieval, and visualization.
GeneCards is an integrated database of human genes that includes automatically-mined genomic, proteomic and transcriptomic information, as well as orthologies, disease relationships, SNPs, gene expression, gene function, and service links for ordering assays and antibodies.
The Genome Variation Server (GVS) is a local database hosted by the SeattleSNPs Program for Genomic Applications (PGA). The objective of this database is to provide a simple tool for rapid access to human genotype data found in dbSNP, and to provide tools for analysis of genotype data.
The Human Genome Variation database of Genotype-to-Phenotype information (HGVbaseG2P) provides a centralized compilation of summary level findings from genetic association studies, both large and small. They actively gather datasets from public domain projects, and encourage direct data submission from the community.
NUGene collects and stores DNA samples along with healthcare information from patients of Northwestern-affiliated hospitals and clinics. This resource is made available to scientists for research purposes.
Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders. OMIM focuses primarily on inherited, or heritable, genetic diseases. It is also considered to be a phenotypic companion to the human genome project.