* Establishes the standards of competence for clinical practice through accreditation of graduate programs in genetic counseling. Advances the role of genetic counselors in healthcare through the certification and recertification of qualified professionals.
ALFRED is a free, web-accessible, curated compilation of allele frequency data on DNA sequence polymorphisms in anthropologically defined human populations. Data in ALFRED are linked to literature, molecular, and ethnographic databases
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.
CarpeDB serves as a novel source for epilepsy researchers by featuring scores of "epilepsy genes" and associated publications in one locus. Furthermore, multiple genes implicated in epilepsy are also implicated in other human disorders.
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.
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.
A collection of conserved sequence elements, identified by a systematic genomic sequence comparison between a set of human genes involved in the pathogenesis of genetic disorders and their murine (mouse) counterparts.
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.
GENATLAS contains relevant information with respect to gene mapping and genetic diseases. GENATLAS is structured in three databases: Genes database, Phenotypes database, Citations database (linked to the two previous). The information is collected from published literature.