This PheWeb contains results from genome-wide association studies (GWAS) of 1542 EHR-derived broad PheWAS codes for approximately 51.8 million imputed variants in 51,583 European-ancestry individuals from the Michigan Genomics Initiative (MGI), a biobank of Michigan Medicine patients. Phenotypes are derived from diagnosis codes extracted from patient Electronic Health Records using the PheWAS R package (https://github.com/PheWAS/PheWAS). Genetic data in MGI participants is imputed using the TOPMed reference panel to provide association testing at high-quality genetic variants for each phenotype. The PheWeb interface allows interactive exploration of individual GWAS as well as phenome-wide association analysis of individual genetic variants.
White paper for the pheweb can be found here
If you would like to request access to this Pheweb, report a bug, or make a suggestion, please email mgipheweb@umich.edu
