rs57989773, None

N. diseases: 2
Disease: Erectile dysfunction ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Erectile dysfunction
CUI: C0242350
Disease: Erectile dysfunction
0.710 GeneticVariation BEFREE We performed a genome-wide association study of ED in 6,175 case subjects among 223,805 European men and identified one locus at 6q16.3 (lead variant rs57989773, OR 1.20 per C-allele; p = 5.71 × 10<sup>-14</sup>), located between MCHR2 and SIM1. 30583798 2019
Erectile dysfunction
CUI: C0242350
Disease: Erectile dysfunction
0.710 GeneticVariation GWASCAT We performed a genome-wide association study of ED in 6,175 case subjects among 223,805 European men and identified one locus at 6q16.3 (lead variant rs57989773, OR 1.20 per C-allele; p = 5.71 × 10<sup>-14</sup>), located between MCHR2 and SIM1. 30583798 2019