Source: CURATED ×
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: rs137852355
rs137852355
F8
1 1.000 0.080 X 154861759 stop gained G/A;C snv 0.800 1.000 2 2011 2013
dbSNP: rs137852359
rs137852359
F8
1 1.000 0.080 X 154969468 missense variant T/C snv 0.800 1.000 2 2011 2013
dbSNP: rs137852360
rs137852360
F8
2 0.925 0.080 X 154837676 missense variant C/A;G;T snv 0.800 1.000 2 2011 2013
dbSNP: rs137852362
rs137852362
F8
1 1.000 0.080 X 154928607 missense variant T/C snv 0.800 1.000 2 2011 2013
dbSNP: rs137852364
rs137852364
F8
1 1.000 0.080 X 154966526 missense variant G/A snv 0.800 1.000 2 2011 2013
dbSNP: rs137852365
rs137852365
F8
1 1.000 0.080 X 154863103 missense variant A/G snv 0.800 1.000 2 2011 2013
dbSNP: rs137852366
rs137852366
F8
1 1.000 0.080 X 154896102 missense variant C/G;T snv 1.6E-05 0.800 1.000 2 2011 2013
dbSNP: rs137852367
rs137852367
F8
1 1.000 0.080 X 154992971 missense variant G/A snv 0.800 1.000 2 2011 2013
dbSNP: rs137852369
rs137852369
F8
1 1.000 0.080 X 154904083 missense variant T/C snv 0.800 1.000 2 2011 2013
dbSNP: rs137852371
rs137852371
F8
1 1.000 0.080 X 154966664 missense variant C/A;G snv 0.800 1.000 2 2011 2013
dbSNP: rs137852373
rs137852373
F8
1 1.000 0.080 X 154928623 stop gained C/A;T snv 0.800 1.000 2 2011 2013
dbSNP: rs137852375
rs137852375
F8
1 1.000 0.080 X 154906421 missense variant A/G snv 0.800 1.000 2 2011 2013
dbSNP: rs137852376
rs137852376
F8
1 1.000 0.080 X 154954041 missense variant A/G snv 0.800 1.000 2 2011 2013
dbSNP: rs137852377
rs137852377
F8
1 1.000 0.080 X 155022476 missense variant A/C snv 0.800 1.000 2 2011 2013
dbSNP: rs137852378
rs137852378
F8
1 1.000 0.080 X 155022464 missense variant T/A snv 0.800 1.000 2 2011 2013
dbSNP: rs137852379
rs137852379
F8
1 1.000 0.080 X 155022432 missense variant C/A;T snv 1.1E-04; 1.1E-05 0.800 1.000 2 2011 2013
dbSNP: rs137852380
rs137852380
F8
1 1.000 0.080 X 154997095 missense variant C/T snv 0.800 1.000 2 2011 2013
dbSNP: rs137852381
rs137852381
F8
1 1.000 0.080 X 154997086 missense variant C/A snv 0.800 1.000 2 2011 2013
dbSNP: rs137852382
rs137852382
F8
1 1.000 0.080 X 154997065 missense variant A/G;T snv 0.800 1.000 2 2011 2013
dbSNP: rs137852383
rs137852383
F8
1 1.000 0.080 X 154997050 missense variant A/C;T snv 0.800 1.000 2 2011 2013
dbSNP: rs137852384
rs137852384
F8
1 1.000 0.080 X 154997038 missense variant T/G snv 0.800 1.000 2 2011 2013
dbSNP: rs137852385
rs137852385
F8
1 1.000 0.080 X 154997033 missense variant T/C snv 0.800 1.000 2 2011 2013
dbSNP: rs137852386
rs137852386
F8
1 1.000 0.080 X 154997011 missense variant A/C snv 0.800 1.000 2 2011 2013
dbSNP: rs137852387
rs137852387
F8
1 1.000 0.080 X 154996973 missense variant C/G snv 0.800 1.000 2 2011 2013
dbSNP: rs137852388
rs137852388
F8
1 1.000 0.080 X 154993141 missense variant T/G snv 1.8E-04 1.8E-04 0.800 1.000 2 2011 2013