rs6061244, GATA5

N. diseases: 2
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 1.000 0.040 20 62466597 intron variant G/A;C snv 1.3E-03; 0.38 0.700 1.000 1 2018 2018
Lower Urinary Tract Symptoms
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
30 1.000 0.040 20 62466597 intron variant G/A;C snv 1.3E-03; 0.38 0.700 1.000 1 2018 2018