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: rs137852422
rs137852422
F8
1 1.000 0.080 X 154956959 missense variant G/T snv 0.800 1.000 22 1989 2013
dbSNP: rs137852425
rs137852425
F8
1 1.000 0.080 X 154953987 missense variant C/A snv 0.800 1.000 22 1989 2013
dbSNP: rs137852426
rs137852426
F8
1 1.000 0.080 X 154953983 stop gained C/G;T snv 0.800 1.000 22 1989 2013
dbSNP: rs137852427
rs137852427
F8
1 1.000 0.080 X 154953981 missense variant T/C;G snv 0.800 1.000 22 1989 2013
dbSNP: rs137852429
rs137852429
F8
1 1.000 0.080 X 154953903 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs137852430
rs137852430
F8
1 1.000 0.080 X 154947853 missense variant A/G snv 0.800 1.000 22 1989 2013
dbSNP: rs137852433
rs137852433
F8
1 1.000 0.080 X 154947823 missense variant G/A snv 0.800 1.000 22 1989 2013
dbSNP: rs137852434
rs137852434
F8
1 1.000 0.080 X 154947782 missense variant A/G snv 0.800 1.000 22 1989 2013
dbSNP: rs137852436
rs137852436
F8
2 0.925 0.080 X 154931623 missense variant C/T snv 5.5E-06 0.800 1.000 22 1989 2013
dbSNP: rs137852439
rs137852439
F8
1 1.000 0.080 X 154928647 stop gained G/A;C;T snv 0.800 1.000 22 1989 2013
dbSNP: rs137852440
rs137852440
F8
1 1.000 0.080 X 154906488 missense variant C/T snv 0.800 1.000 22 1989 2013
dbSNP: rs137852441
rs137852441
F8
1 1.000 0.080 X 154906468 missense variant C/G snv 0.800 1.000 22 1989 2013
dbSNP: rs137852443
rs137852443
F8
1 1.000 0.080 X 154904999 missense variant G/A;C snv 5.5E-06 0.800 1.000 22 1989 2013
dbSNP: rs137852444
rs137852444
F8
1 1.000 0.080 X 154904989 missense variant G/A;T snv 0.800 1.000 22 1989 2013
dbSNP: rs137852445
rs137852445
F8
1 1.000 0.080 X 154904975 missense variant G/A snv 0.800 1.000 22 1989 2013
dbSNP: rs137852450
rs137852450
F8
1 1.000 0.080 X 154903968 missense variant C/A snv 0.800 1.000 22 1989 2013
dbSNP: rs137852451
rs137852451
F8
1 1.000 0.080 X 154903966 missense variant G/A snv 0.800 1.000 22 1989 2013
dbSNP: rs137852453
rs137852453
F8
1 1.000 0.080 X 154902120 missense variant G/A snv 0.800 1.000 22 1989 2013
dbSNP: rs137852454
rs137852454
F8
1 1.000 0.080 X 154902053 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs137852455
rs137852455
F8
1 1.000 0.080 X 154899946 missense variant A/G snv 0.800 1.000 22 1989 2013
dbSNP: rs137852456
rs137852456
F8
1 1.000 0.080 X 154899876 missense variant G/A;T snv 0.800 1.000 22 1989 2013
dbSNP: rs137852457
rs137852457
F8
1 1.000 0.080 X 154896228 missense variant T/A;C snv 0.800 1.000 22 1989 2013
dbSNP: rs137852458
rs137852458
F8
1 1.000 0.080 X 154896146 missense variant A/C snv 0.800 1.000 22 1989 2013
dbSNP: rs137852459
rs137852459
F8
2 0.925 0.080 X 154896135 missense variant T/C snv 5.5E-06 0.800 1.000 22 1989 2013
dbSNP: rs137852460
rs137852460
F8
1 1.000 0.080 X 154896093 missense variant G/T snv 0.800 1.000 22 1989 2013