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: rs1375894900
rs1375894900
F8
1 1.000 0.080 X 154930696 frameshift variant TTCT/- delins 0.700 0
dbSNP: rs387906454
rs387906454
F8
1 1.000 0.080 X 154929459 frameshift variant TTCT/- delins 0.700 0
dbSNP: rs387906433
rs387906433
F8
1 1.000 0.080 X 154999544 frameshift variant TT/-;TTT delins 0.700 0
dbSNP: rs387906449
rs387906449
F8
1 1.000 0.080 X 154930241 frameshift variant TT/-;TTT delins 0.700 0
dbSNP: rs1557278778
rs1557278778
F8
1 1.000 0.080 X 154931055 frameshift variant TT/- del 0.700 0
dbSNP: rs387906441
rs387906441
F8
1 1.000 0.080 X 154966499 frameshift variant TT/- delins 0.700 0
dbSNP: rs387906463
rs387906463
F8
1 1.000 0.080 X 154863192 frameshift variant TT/- delins 0.700 0
dbSNP: rs387906440
rs387906440
F8
1 1.000 0.080 X 154966618 frameshift variant TC/- del 0.700 0
dbSNP: rs28933676
rs28933676
F8
1 1.000 0.080 X 154904864 missense variant T/G snv 0.800 1.000 22 1989 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: 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
dbSNP: rs137852395
rs137852395
F8
1 1.000 0.080 X 154992983 missense variant T/G snv 0.800 1.000 2 2011 2013
dbSNP: rs397507444
rs397507444
MTHFR
306 0.405 0.880 1 11794407 missense variant T/G snv 0.020 1.000 2 2008 2014
dbSNP: rs8099917
rs8099917 		60 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.010 1.000 1 2013 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: rs137852406
rs137852406
F8
2 0.925 0.080 X 154969400 missense variant T/C snv 5.5E-06 0.810 1.000 23 1989 2014
dbSNP: rs137852420
rs137852420
F8
1 1.000 0.080 X 154957027 missense variant T/C 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: rs137852454
rs137852454
F8
1 1.000 0.080 X 154902053 missense variant T/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: rs137852470
rs137852470
F8
1 1.000 0.080 X 154860538 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs137852476
rs137852476
F8
1 1.000 0.080 X 155022449 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs28933671
rs28933671
F8
1 1.000 0.080 X 154966471 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs28933679
rs28933679
F8
1 1.000 0.080 X 154904511 missense variant T/C snv 0.800 1.000 22 1989 2013
dbSNP: rs28933682
rs28933682
F8
1 1.000 0.080 X 154904082 missense variant T/C snv 0.800 1.000 22 1989 2013