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: rs137852412
rs137852412
F8
2 0.925 0.080 X 154961137 missense variant T/C snv 0.010 1.000 1 2013 2013
dbSNP: rs137852464
rs137852464
F8
2 0.925 0.080 X 154863125 missense variant G/A snv 0.010 1.000 1 1997 1997
dbSNP: rs753654616
rs753654616
F9
2 0.925 0.080 X 139561530 missense variant A/G snv 0.010 1.000 1 2011 2011
dbSNP: rs772061412
rs772061412
F9
2 0.925 0.080 X 139561664 missense variant C/G snv 5.5E-06 0.010 1.000 1 2011 2011
dbSNP: rs782426204
rs782426204
F8
2 1.000 0.080 X 154904974 missense variant A/G snv 5.5E-06 0.010 < 0.001 1 2015 2015
dbSNP: rs782548763
rs782548763
F8
2 0.925 0.080 X 154861783 missense variant C/G snv 5.5E-06 0.010 1.000 1 2007 2007