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: rs8853
rs8853
0.882 0.120 12 114671102 3 prime UTR variant T/C snv 0.52
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia
0.700 1.000 1 2018 2018
dbSNP: rs8853
rs8853
0.882 0.120 12 114671102 3 prime UTR variant T/C snv 0.52
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
Lower Urinary Tract Symptoms
0.700 1.000 1 2018 2018
dbSNP: rs8853
rs8853
0.882 0.120 12 114671102 3 prime UTR variant T/C snv 0.52
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs8853
rs8853
0.882 0.120 12 114671102 3 prime UTR variant T/C snv 0.52
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2016 2016