Results displayed in this PheWeb include genome-wide associations for EHR-derived ICD-9 billing codes from participants of the Michigan Genomics Initiative. Phenotypes were classified into 1,448 broad PheWAS codes with counts ranging from 20 – 6,083 cases and 5,733 – 18,219 controls. All individuals were genotyped on the Illumina HumanCoreExome Array and imputed using the Haplotype Reference Consortium panel, resulting in ~8 million common variants. Associations were carried out on binary outcomes using a saddlepoint approximation test with adjustment for age, sex, and principal components 1-4. All genomic positions are on GRCh37.