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: 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: 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: 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: 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: 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: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.710 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: rs7405776
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 1.000 1 2017 2017
dbSNP: rs7405776
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma 		0.700 1.000 1 2017 2017
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: rs7501939
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.740 1.000 4 2008 2018
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: 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: 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: 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: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 1.000 1 2012 2018
dbSNP: rs17138478
rs17138478
HNF1B ; LOC105371754
17 37713312 intron variant C/A;T snv 0.11
CUI: C0242216
Disease: Biliary calculi
Biliary calculi 		0.700 1.000 1 2018 2018
dbSNP: rs4795218
rs4795218
HNF1B ; LOC105371754
0.925 0.120 17 37718512 intron variant A/G snv 0.82
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.710 < 0.001 1 2018 2018
dbSNP: rs4430796
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.800 1.000 5 2007 2019
dbSNP: rs4430796
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.870 1.000 3 2009 2019
dbSNP: rs11649743
rs11649743
HNF1B ; LOC105371754
0.925 0.080 17 37714971 intron variant A/G snv 0.85
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.730 1.000 2 2011 2019
dbSNP: rs11651052
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 1.000 2 2012 2019