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: rs778986
rs778986
3 1.000 0.080 19 5844526 missense variant A/G snv 0.84 0.84 0.010 1.000 1 2016 2016
dbSNP: rs812936
rs812936
2 1.000 0.080 19 5844638 missense variant G/A;C snv 0.83 0.010 1.000 1 2016 2016