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: rs2941471
rs2941471
HNF4G
4 0.851 0.240 8 75558169 intron variant G/A snv 0.65 0.010 < 0.001 1 2018 2018