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: rs11651755
rs11651755
HNF1B
9 0.763 0.160 17 37739849 intron variant T/C snv 0.52 0.700 1.000 1 2017 2017
dbSNP: rs7405776
rs7405776
HNF1B
6 0.807 0.120 17 37733029 intron variant G/A;C snv 0.700 1.000 1 2017 2017