• 1. AlzGene database
• The AlzGene database aims to provide a comprehensive, unbiased and regularly updated collection of genetic association studies performed on Alzheimer’s disease phenotypes.

• 2. Blood Group Antigen Gene Mutation Database (dbRBC)
• NCBI. The Blood Group Antigen Gene Mutation Database (dbRBC) documents variations in genes that directly or indirectly affect blood groups. It thus is a locus-specific mutation database (LSDB) that covers multiple genes.

• 3. CGAP and CGCI - Cancer Genome Anatomy Project & Cancer Genome Characterization Initiative
• The goal of the NCI's Cancer Genome Anatomy Project is to determine the gene expression profiles of normal, precancer, and cancer cells, leading eventually to improved detection, diagnosis, and treatment for the patient. Includes high-quality histology photos of tissue expression.

• 4. Database of Genomic Variants
• A comprehensive summary of structural variation in the human genome.

• 5. dbGaP
• 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.

• 6. ENCODE Project at UCSC
• 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.

• 7. G2D: Candidate Genes to Inherited Diseases
• The Genes2Diseases server presents precomputed candidate genes for more than 600 genetically inherited diseases that have been mapped onto chromosomal regions without assignment of a particular gene.

• 8. Genome Browsers and Tools Resource List
• Galter Library-created list of genome browsers and genome analysis servers

• 9. Genome Variation Server
• 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.

• 10. HGVbaseG2P: a Human Genome Variation and Genotype/Phenotype Database
• 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.

• 11. HGVS; Human Genome Variation Society's Variation Databases and Related sites
• The HGVS' list of variation databases includes SNP and locus specific databases. Users are encouraged to check the currency of databases when using them.

• 12. MutDB
• The goal of MutDB is to annotate human variation data with protein structural information and other functionally relevant information, if available. The mutations are organized by gene.

• 13. NUgene Project
• 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.

• 14. OMIM
• 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.

• 15. UCSC Genome Browser Home
• The UCSC Genome Browser contains the reference sequence and working draft assemblies for a large collection of genomes. It also provides portals to the ENCODE and Neandertal projects