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: rs121913076
rs121913076
FAS
2 0.925 0.120 10 89014163 missense variant A/C snv 0.700 1.000 13 1995 2010
dbSNP: rs121913078
rs121913078
FAS
2 0.925 0.120 10 89008915 missense variant C/T snv 4.0E-06 0.700 1.000 13 1995 2010
dbSNP: rs121913079
rs121913079
FAS
1 1.000 0.120 10 89014137 missense variant A/G snv 0.700 1.000 13 1995 2010
dbSNP: rs121913080
rs121913080
FAS
3 0.882 0.160 10 89014191 missense variant G/C snv 0.700 1.000 13 1995 2010
dbSNP: rs121913081
rs121913081
FAS
2 0.925 0.120 10 89014251 missense variant C/T snv 0.700 1.000 13 1995 2010
dbSNP: rs121913086
rs121913086
FAS
2 0.925 0.120 10 89014220 missense variant G/T snv 0.700 1.000 13 1995 2010
dbSNP: rs201072885
rs201072885
FAS
1 1.000 0.120 10 89014164 missense variant C/A snv 6.0E-05 0.700 1.000 13 1995 2010
dbSNP: rs1564691414
rs1564691414
FAS
7 0.925 0.160 10 89007698 splice acceptor variant A/G snv 0.700 0
dbSNP: rs1564696849
rs1564696849
FAS
2 0.925 0.160 10 89012082 splice donor variant G/A snv 0.700 0
dbSNP: rs28929498
rs28929498
FAS
2 0.925 0.120 10 89014221 missense variant A/T snv 0.700 0