Source: BEFREE

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
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 16 2007 2019
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: 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 3 2011 2019
dbSNP: rs3760511
rs3760511
HNF1B
0.925 0.080 17 37746322 upstream gene variant G/A;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.020 1.000 2 2016 2018
dbSNP: rs4794758
rs4794758
HNF1B ; LOC105371754
0.925 0.080 17 37720433 intron variant T/C snv 0.66
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs757210
rs757210
HNF1B
0.807 0.160 17 37736525 intron variant C/G;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2012 2012