Gene: HNF1B ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4430796
rs4430796
HNF1B
14 0.790 0.280 17 37738049 intron variant A/G snv 0.52 0.800 1.000 18 2008 2018
dbSNP: rs7501939
rs7501939
HNF1B
12 0.776 0.280 17 37741165 intron variant C/T snv 0.41 0.740 1.000 8 2008 2018
dbSNP: rs3760511
rs3760511
HNF1B
2 0.925 0.080 17 37746322 upstream gene variant G/A;T snv 0.720 1.000 3 2008 2018
dbSNP: rs3744763
rs3744763
HNF1B
3 0.925 0.160 17 37730894 non coding transcript exon variant A/G snv 0.30 0.700 1.000 1 2008 2008
dbSNP: rs11649743
rs11649743
HNF1B ; LOC105371754
2 0.925 0.080 17 37714971 intron variant A/G snv 0.85 0.030 1.000 3 2011 2018
dbSNP: rs4794758
rs4794758
HNF1B ; LOC105371754
2 0.925 0.080 17 37720433 intron variant T/C snv 0.66 0.010 1.000 1 2011 2011
dbSNP: rs757210
rs757210
HNF1B
6 0.807 0.160 17 37736525 intron variant C/G;T snv 0.010 1.000 1 2012 2012