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 0.870 1.000 11 2009 2019
dbSNP: rs121918673
rs121918673
HNF1B
3 0.925 0.200 17 37701122 missense variant G/C snv 1.9E-05 0.810 1.000 3 2002 2013
dbSNP: rs11651052
rs11651052
HNF1B
7 0.851 0.200 17 37742390 intron variant G/A snv 0.50 0.800 1.000 2 2012 2019
dbSNP: rs11651755
rs11651755
HNF1B
9 0.763 0.160 17 37739849 intron variant T/C snv 0.52 0.800 1.000 2 2012 2018
dbSNP: rs7501939
rs7501939
HNF1B
12 0.776 0.280 17 37741165 intron variant C/T snv 0.41 0.720 1.000 3 2010 2019
dbSNP: rs10908278
rs10908278
HNF1B
2 0.925 0.160 17 37739961 intron variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11263763
rs11263763
HNF1B
6 0.882 0.200 17 37743574 intron variant A/G snv 0.43 0.700 1.000 1 2012 2012
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 2011 2011
dbSNP: rs121918672
rs121918672
HNF1B
2 0.925 0.200 17 37731814 stop gained G/A snv 0.010 1.000 1 2002 2002
dbSNP: rs2229295
rs2229295
HNF1B ; LOC105371755
1 1.000 0.080 17 37687273 3 prime UTR variant G/A;T snv 4.0E-06; 0.19 0.010 1.000 1 2015 2015