rs10054105, STARD4-AS1

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 5 111573636 intron variant T/G snv 0.17 0.700 1.000 1 2018 2018
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.925 0.080 5 111573636 intron variant T/G snv 0.17 0.700 1.000 1 2017 2017
Lower Urinary Tract Symptoms
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
30 0.925 0.080 5 111573636 intron variant T/G snv 0.17 0.700 1.000 1 2018 2018