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: rs4430796
rs4430796
0.790 0.280 17 37738049 intron variant A/G snv 0.52
Diabetes Mellitus, Non-Insulin-Dependent
0.870 1.000 3 2009 2019
dbSNP: rs4430796
rs4430796
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: rs11651052
rs11651052
0.851 0.200 17 37742390 intron variant G/A snv 0.50
Diabetes Mellitus, Non-Insulin-Dependent
0.800 1.000 2 2012 2019
dbSNP: rs11263763
rs11263763
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
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: rs11651755
rs11651755
0.763 0.160 17 37739849 intron variant T/C snv 0.52
Diabetes Mellitus, Non-Insulin-Dependent
0.800 1.000 1 2012 2018
dbSNP: rs4430796
rs4430796
0.790 0.280 17 37738049 intron variant A/G snv 0.52
Prostate specific antigen measurement
0.800 1.000 1 2010 2010
dbSNP: rs7501939
rs7501939
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: rs11649743
rs11649743
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: rs7501939
rs7501939
0.776 0.280 17 37741165 intron variant C/T snv 0.41
Diabetes Mellitus, Non-Insulin-Dependent
0.720 1.000 1 2010 2019
dbSNP: rs11651755
rs11651755
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: rs4795218
rs4795218
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: rs757210
rs757210
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: rs7501939
rs7501939
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
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
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
0.925 0.160 17 37739961 intron variant A/C;T snv
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 1 2016 2016
dbSNP: rs11263761
rs11263761
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
1.000 0.080 17 37737784 intron variant A/G snv 0.44
Prostate specific antigen measurement
0.700 1.000 1 2017 2017
dbSNP: rs11263763
rs11263763
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
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
0.851 0.200 17 37742390 intron variant G/A snv 0.50
Prostate specific antigen measurement
0.700 1.000 1 2018 2018
dbSNP: rs11651052
rs11651052
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
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
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