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: rs12921862
rs12921862
0.763 0.200 16 331927 intron variant C/A snv 0.18
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs12921862
rs12921862
0.763 0.200 16 331927 intron variant C/A snv 0.18
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.010 1.000 1 2019 2019
dbSNP: rs12921862
rs12921862
0.763 0.200 16 331927 intron variant C/A snv 0.18
Malignant neoplasm of urinary bladder
0.010 1.000 1 2019 2019
dbSNP: rs12921862
rs12921862
0.763 0.200 16 331927 intron variant C/A snv 0.18
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.010 1.000 1 2019 2019
dbSNP: rs12921862
rs12921862
0.763 0.200 16 331927 intron variant C/A snv 0.18
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
0.010 1.000 1 2019 2019
dbSNP: rs12921862
rs12921862
0.763 0.200 16 331927 intron variant C/A snv 0.18
Carcinoma of urinary bladder, invasive
0.010 1.000 1 2019 2019
dbSNP: rs12921862
rs12921862
0.763 0.200 16 331927 intron variant C/A snv 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2019 2019
dbSNP: rs12921862
rs12921862
0.763 0.200 16 331927 intron variant C/A snv 0.18
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
0.010 1.000 1 2019 2019
dbSNP: rs12921862
rs12921862
0.763 0.200 16 331927 intron variant C/A snv 0.18
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.010 1.000 1 2019 2019
dbSNP: rs12921862
rs12921862
0.763 0.200 16 331927 intron variant C/A snv 0.18
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer
0.010 1.000 1 2019 2019