Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10054105
rs10054105
0.925 0.080 5 111573636 intron variant T/G snv 0.17
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
Lower Urinary Tract Symptoms
0.700 1.000 1 2018 2018
dbSNP: rs10054105
rs10054105
0.925 0.080 5 111573636 intron variant T/G snv 0.17
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia
0.700 1.000 1 2018 2018
dbSNP: rs10054105
rs10054105
0.925 0.080 5 111573636 intron variant T/G snv 0.17
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017