Gene: F9 ×
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: rs387906481
rs387906481
F9
1 1.000 0.080 X 139530846 missense variant T/C snv 0.800 1.000 22 1983 2015
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: rs1275708479
rs1275708479
F9
1 1.000 0.080 X 139537049 missense variant G/A;T snv 0.700 1.000 20 1983 2015
dbSNP: rs137852226
rs137852226
F9
1 1.000 0.080 X 139537139 missense variant A/T snv 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: rs137852240
rs137852240
F9
1 1.000 0.080 X 139551217 missense variant C/T snv 0.800 1.000 2 2012 2013
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
dbSNP: rs137852249
rs137852249
F9
1 0.882 0.080 X 139561566 missense variant G/A snv 0.810 1.000 2 1989 2018
dbSNP: rs137852251
rs137852251
F9
1 1.000 0.080 X 139561602 missense variant A/G snv 0.800 1.000 2 2012 2013
dbSNP: rs137852258
rs137852258
F9
1 1.000 0.080 X 139561820 stop gained C/G;T snv 0.800 1.000 2 2012 2013
dbSNP: rs137852259
rs137852259
F9
1 0.925 0.080 X 139561821 missense variant G/A snv 0.800 1.000 2 2012 2013
dbSNP: rs137852266
rs137852266
F9
1 1.000 0.080 X 139561992 missense variant C/A;T snv 0.800 1.000 2 2012 2013
dbSNP: rs137852267
rs137852267
F9
1 1.000 0.080 X 139562009 missense variant G/A snv 0.800 1.000 2 2012 2013
dbSNP: rs137852268
rs137852268
F9
1 1.000 0.080 X 139562013 missense variant T/C snv 0.800 1.000 2 2012 2013
dbSNP: rs137852269
rs137852269
F9
1 1.000 0.080 X 139562042 missense variant T/C snv 0.800 1.000 2 2012 2013
dbSNP: rs137852273
rs137852273
F9
1 1.000 0.080 X 139561872 missense variant G/A;C snv 0.800 1.000 2 2012 2013
dbSNP: rs137852274
rs137852274
F9
1 1.000 0.080 X 139541126 missense variant G/A snv 0.800 1.000 2 2012 2013
dbSNP: rs137852275
rs137852275
F9
1 1.000 0.080 X 139561755 missense variant G/A snv 0.800 1.000 2 2012 2013
dbSNP: rs137852276
rs137852276
F9
1 1.000 0.080 X 139561917 missense variant G/T snv 0.800 1.000 2 2012 2013
dbSNP: rs137852277
rs137852277
F9
1 1.000 0.080 X 139561916 missense variant A/G snv 0.800 1.000 2 2012 2013
dbSNP: rs137852278
rs137852278
F9
1 1.000 0.080 X 139561913 missense variant G/C snv 0.800 1.000 2 2012 2013