Source: UNIPROT ×
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: rs1170838100
rs1170838100
F9
1 1.000 0.080 X 139561979 missense variant G/A snv 0.700 0
dbSNP: rs1175050951
rs1175050951
F9
1 1.000 0.080 X 139561868 missense variant T/A;C snv 0.700 0
dbSNP: rs1182648920
rs1182648920
F9
1 1.000 0.080 X 139551264 missense variant G/T snv 0.700 0
dbSNP: rs1216516070
rs1216516070
F9
1 1.000 0.080 X 139548387 missense variant G/A snv 0.700 1.000 20 1983 2015
dbSNP: rs1222227572
rs1222227572
F9
1 1.000 0.080 X 139561638 missense variant T/G snv 0.700 1.000 20 1983 2015
dbSNP: rs1233706534
rs1233706534
F9
1 1.000 0.080 X 139561920 missense variant G/A snv 0.700 0
dbSNP: rs1243180674
rs1243180674
F9
1 1.000 0.080 X 139562034 missense variant A/G snv 0.700 0
dbSNP: rs1275708479
rs1275708479
F9
1 1.000 0.080 X 139537049 missense variant G/A;T snv 0.700 1.000 20 1983 2015
dbSNP: rs1303221289
rs1303221289
F9
1 1.000 0.080 X 139561830 missense variant G/A snv 0.700 0
dbSNP: rs1306658513
rs1306658513
F9
1 1.000 0.080 X 139561922 missense variant G/C snv 0.700 0
dbSNP: rs1330705989
rs1330705989
F9
1 1.000 0.080 X 139548435 missense variant G/C;T snv 0.700 0
dbSNP: rs137852225
rs137852225
F9
1 1.000 0.080 X 139537138 missense variant G/A snv 0.700 0
dbSNP: rs137852226
rs137852226
F9
1 1.000 0.080 X 139537139 missense variant A/T snv 0.800 1.000 2 2012 2013
dbSNP: rs137852228
rs137852228
F9
1 0.925 0.080 X 139537145 missense variant G/A snv 5.5E-06 0.800 1.000 2 2012 2013
dbSNP: rs137852229
rs137852229
F9
1 1.000 0.080 X 139537158 missense variant A/C snv 0.800 1.000 2 2012 2013
dbSNP: rs137852230
rs137852230
F9
1 1.000 0.080 X 139541076 missense variant A/G snv 0.800 1.000 2 2012 2013
dbSNP: rs137852231
rs137852231
F9
1 1.000 0.080 X 139541085 splice acceptor variant A/C snv 0.800 1.000 2 2012 2013
dbSNP: rs137852233
rs137852233
F9
1 0.925 0.080 X 139541114 missense variant G/A snv 1.1E-05 3.8E-05 0.800 1.000 2 1989 2013
dbSNP: rs137852237
rs137852237
F9
1 1.000 0.080 X 139551112 missense variant C/A;T snv 5.5E-06 0.810 1.000 2 2012 2016
dbSNP: rs137852238
rs137852238
F9
1 0.925 0.080 X 139551113 missense variant G/A snv 5.5E-06 9.5E-06 0.800 1.000 2 2012 2013
dbSNP: rs137852240
rs137852240
F9
1 1.000 0.080 X 139551217 missense variant C/T snv 0.800 1.000 2 2012 2013
dbSNP: rs137852241
rs137852241
F9
1 1.000 0.080 X 139551218 missense variant G/A snv 0.800 0
dbSNP: rs137852242
rs137852242
F9
1 1.000 0.080 X 139551220 missense variant G/A;T snv 6.5E-05 0.700 0
dbSNP: rs137852243
rs137852243
F9
1 1.000 0.080 X 139551223 missense variant G/A;C;T snv 0.800 1.000 2 2012 2013
dbSNP: rs137852246
rs137852246
F9
1 1.000 0.080 X 139560821 missense variant T/G snv 0.800 1.000 2 2012 2013