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: rs7501939
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor 		0.700 1.000 3 2015 2017
dbSNP: rs11651052
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.700 1.000 2 2016 2018
dbSNP: rs3110641
rs3110641
HNF1B ; LOC105371755
17 37687414 intron variant G/A snv 0.32
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 2 2018 2019
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: rs11263761
rs11263761
HNF1B
1.000 0.080 17 37737784 intron variant A/G snv 0.44
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.700 1.000 1 2018 2018
dbSNP: rs11263761
rs11263761
HNF1B
1.000 0.080 17 37737784 intron variant A/G snv 0.44
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0.700 1.000 1 2017 2017
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: rs11651052
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
Lower Urinary Tract Symptoms 		0.700 1.000 1 2018 2018
dbSNP: rs11651052
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11651052
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs11651052
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia 		0.700 1.000 1 2018 2018
dbSNP: rs11651755
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52
CUI: C1518693
Disease: Clear cell adenocarcinoma of ovary
Clear cell adenocarcinoma of ovary 		0.700 1.000 1 2017 2017
dbSNP: rs11651755
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs11658063
rs11658063
HNF1B
0.851 0.120 17 37743881 intron variant G/C;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
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