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: rs7224610
rs7224610
HLF
4 0.925 0.120 17 55287427 intron variant C/A;G snv 0.700 1.000 2 2013 2019
dbSNP: rs3794748
rs3794748
HLF
3 0.925 0.120 17 55287811 intron variant A/G snv 0.69 0.700 1.000 1 2019 2019