Source: GWASCAT

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: rs7405776
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv
CUI: C1518693
Disease: Clear cell adenocarcinoma of ovary
Clear cell adenocarcinoma of ovary 		0.700 1.000 1 2017 2017
dbSNP: rs10908278
rs10908278
HNF1B
0.925 0.160 17 37739961 intron variant A/C;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2016 2016
dbSNP: rs11263763
rs11263763
HNF1B
0.882 0.200 17 37743574 intron variant A/G snv 0.43
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.800 1.000 1 2011 2016
dbSNP: rs11651052
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.800 1.000 1 2011 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C0346163
Disease: Endometrioid carcinoma ovary
Endometrioid carcinoma ovary 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs12601991
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 1.000 1 2016 2016
dbSNP: rs11263763
rs11263763
HNF1B
0.882 0.200 17 37743574 intron variant A/G snv 0.43
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2015 2015
dbSNP: rs757210
rs757210
HNF1B
0.807 0.160 17 37736525 intron variant C/G;T snv
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer 		0.710 1.000 1 2013 2015
dbSNP: rs8064454
rs8064454
HNF1B
0.925 0.120 17 37741595 intron variant C/A;G snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2015 2015
dbSNP: rs2005705
rs2005705
HNF1B
0.925 0.120 17 37736310 intron variant G/A snv 0.46
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 1 2014 2014