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: rs879036238
rs879036238
1 1.000 1 228097217 missense variant T/C snv 0.800 1.000 1 2016 2016
dbSNP: rs1558087712
rs1558087712
1 1.000 1 228097627 missense variant G/A snv 0.700 0
dbSNP: rs1558087795
rs1558087795
1 1.000 1 228097710 missense variant A/G snv 0.700 0