rs12921862, AXIN1

N. diseases: 10
Source: BEFREE ×
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.
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
278 0.763 0.200 16 331927 intron variant C/A snv 0.18 0.010 1.000 1 2019 2019
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
290 0.763 0.200 16 331927 intron variant C/A snv 0.18 0.010 1.000 1 2019 2019
Carcinoma of urinary bladder, invasive
14 0.763 0.200 16 331927 intron variant C/A snv 0.18 0.010 1.000 1 2019 2019
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
321 0.763 0.200 16 331927 intron variant C/A snv 0.18 0.010 1.000 1 2019 2019
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
200 0.763 0.200 16 331927 intron variant C/A snv 0.18 0.010 1.000 1 2019 2019
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
40 0.763 0.200 16 331927 intron variant C/A snv 0.18 0.010 1.000 1 2019 2019
Conventional (Clear Cell) Renal Cell Carcinoma
203 0.763 0.200 16 331927 intron variant C/A snv 0.18 0.010 1.000 1 2017 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
769 0.763 0.200 16 331927 intron variant C/A snv 0.18 0.010 1.000 1 2019 2019
Epithelial ovarian cancer
CUI: C0677886
Disease: Epithelial ovarian cancer
109 0.763 0.200 16 331927 intron variant C/A snv 0.18 0.010 1.000 1 2019 2019
Malignant neoplasm of urinary bladder
289 0.763 0.200 16 331927 intron variant C/A snv 0.18 0.010 1.000 1 2019 2019