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: rs1554851718
rs1554851718
FAS
1 10 89010783 missense variant T/G snv 0.700 0
dbSNP: rs1564691414
rs1564691414
FAS
7 0.925 0.160 10 89007698 splice acceptor variant A/G snv 0.700 0