rs200383755, GATA5

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.925 0.080 20 62475466 missense variant G/C snv 3.4E-03 3.0E-03 0.700 1.000 1 2018 2018
Lower Urinary Tract Symptoms
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
30 0.925 0.080 20 62475466 missense variant G/C snv 3.4E-03 3.0E-03 0.700 1.000 1 2018 2018
Bicuspid aortic valve
CUI: C0149630
Disease: Bicuspid aortic valve
23 0.925 0.080 20 62475466 missense variant G/C snv 3.4E-03 3.0E-03 0.010 1.000 1 2012 2012