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: rs1057519973
rs1057519973
1 1.000 0.120 8 73946733 missense variant T/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519974
rs1057519974
1 1.000 0.120 8 73946734 missense variant A/T snv 0.700 1.000 1 2016 2016