Source: ALL
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: rs121913088
rs121913088
FGG
2 0.925 0.080 4 154606932 missense variant C/T snv 8.0E-06 0.700 1.000 4 1986 2005
dbSNP: rs121913089
rs121913089
FGG
1 1.000 0.080 4 154606881 missense variant C/A snv 0.700 1.000 4 1986 2005
dbSNP: rs121913094
rs121913094
FGG
1 1.000 0.080 4 154606767 missense variant T/A snv 0.700 1.000 4 1986 2005
dbSNP: rs587777720
rs587777720
FGG
2 0.925 0.080 4 154604986 missense variant A/G snv 0.700 1.000 4 1986 2005
dbSNP: rs121909606
rs121909606
FGA
2 0.925 0.080 4 154589514 missense variant G/A snv 4.0E-06 7.0E-06 0.700 1.000 2 1993 2006
dbSNP: rs121909613
rs121909613
FGA
5 0.882 0.160 4 154585712 splice acceptor variant G/A;C;T snv 4.8E-05; 4.0E-06 0.700 1.000 2 1993 2006
dbSNP: rs121909620
rs121909620
FGB
1 1.000 0.080 4 154565985 missense variant G/A snv 0.700 1.000 1 1992 1992
dbSNP: rs121913091
rs121913091
FGG
1 1.000 0.080 4 154606827 missense variant A/G snv 0.010 1.000 1 2009 2009