rs11084596, None

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.
Prostate specific antigen measurement
95 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 0.700 1.000 2 2017 2018
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 0.700 1.000 1 2018 2018
Lower Urinary Tract Symptoms
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
30 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 0.700 1.000 1 2018 2018