The Phenotype-Genotype Integrator (PheGenI), merges NHGRI
genome-wide association study (GWAS) catalog data with several
databases housed at the National Center for Biotechnology
Information (NCBI), including Gene, dbGaP, OMIM, eQTL and
dbSNP. This phenotype-oriented resource, intended
for clinicians and epidemiologists interested in following
up results from GWAS, can facilitate prioritization of
variants to follow up, study design considerations, and
generation of biological hypotheses. Users can search
based on chromosomal location, gene, SNP, or phenotype and
view and download results including annotated tables of SNPs,
genes and association results, a dynamic genomic sequence
viewer, and gene expression data. PheGenI is still under active
development. Currently, the phenotype search terms are based
on MeSH and will be enhanced with additional options in
the future.
Download
all association results or enter search criteria below.