Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137852246
rs137852246
F9
1.000 0.080 X 139560821 missense variant T/G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852251
rs137852251
F9
1.000 0.080 X 139561602 missense variant A/G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852258
rs137852258
F9
1.000 0.080 X 139561820 stop gained C/G;T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852265
rs137852265
F9
1.000 0.080 X 139561925 missense variant C/A;T snv 5.5E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852266
rs137852266
F9
1.000 0.080 X 139561992 missense variant C/A;T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852267
rs137852267
F9
1.000 0.080 X 139562009 missense variant G/A snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852268
rs137852268
F9
1.000 0.080 X 139562013 missense variant T/C snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852269
rs137852269
F9
1.000 0.080 X 139562042 missense variant T/C snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852273
rs137852273
F9
1.000 0.080 X 139561872 missense variant G/A;C snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852274
rs137852274
F9
1.000 0.080 X 139541126 missense variant G/A snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852275
rs137852275
F9
1.000 0.080 X 139561755 missense variant G/A snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852276
rs137852276
F9
1.000 0.080 X 139561917 missense variant G/T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852277
rs137852277
F9
1.000 0.080 X 139561916 missense variant A/G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852278
rs137852278
F9
1.000 0.080 X 139561913 missense variant G/C snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852279
rs137852279
F9
1.000 0.080 X 139561557 missense variant A/T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852280
rs137852280
F9
1.000 0.080 X 139561941 missense variant T/A;G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852281
rs137852281
F9
1.000 0.080 X 139561874 missense variant G/C snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs267606792
rs267606792
F9
1.000 0.080 X 139560772 missense variant G/C snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852248
rs137852248
F9
1.000 0.080 X 139561565 stop gained C/A;T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.710 1.000 1 2012 2012
dbSNP: rs144314232
rs144314232
F9
1.000 0.080 X 139548430 synonymous variant G/A snv 5.5E-06 9.5E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2017 2017
dbSNP: rs147567879
rs147567879
F9
1.000 0.080 X 139561733 missense variant T/G snv 4.9E-05
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2013 2013
dbSNP: rs1556006174
rs1556006174
F9
1.000 0.080 X 139548489 frameshift variant -/A delins
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2018 2018
dbSNP: rs1556008316
rs1556008316
F9
1.000 0.080 X 139560773 missense variant T/G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2018 2018
dbSNP: rs1556435929
rs1556435929
F9
1.000 0.080 X 139537062 stop gained T/A snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2018 2018
dbSNP: rs387906482
rs387906482
F9
1.000 0.080 X 139561716 missense variant T/C snv 9.4E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.710 1.000 1 2000 2000