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: rs121913082
rs121913082
FAS
2 1.000 0.040 10 89014205 missense variant A/G snv 0.700 0
dbSNP: rs121913083
rs121913083
FAS
2 1.000 0.040 10 89008907 missense variant A/G snv 0.700 0
dbSNP: rs121913084
rs121913084
FAS
2 1.000 0.040 10 89010779 missense variant T/C snv 0.700 0