Source: ALL

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: 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: rs137852229
rs137852229
F9
1.000 0.080 X 139537158 missense variant A/C snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs137852231
rs137852231
F9
1.000 0.080 X 139541085 splice acceptor variant A/C snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.800 1.000 2 2012 2013
dbSNP: rs371045754
rs371045754
F9
0.882 0.200 X 139530726 upstream gene variant A/C snv 5.5E-06 1.9E-05
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2015 2015
dbSNP: rs137852230
rs137852230
F9
1.000 0.080 X 139541076 missense variant A/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: 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: rs137852405
rs137852405
F8
0.925 0.080 X 154969405 missense variant A/G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs72661131
rs72661131
0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2015 2015
dbSNP: rs753654616
rs753654616
F9
0.925 0.080 X 139561530 missense variant A/G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2011 2011
dbSNP: rs766182641
rs766182641
AK3
0.882 0.080 9 4719292 missense variant A/G snv 4.0E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2003 2003
dbSNP: rs1243180674
rs1243180674
F9
1.000 0.080 X 139562034 missense variant A/G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 0
dbSNP: rs137852234
rs137852234
F9
1.000 0.080 X 139541127 missense variant A/G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 0
dbSNP: rs137852262
rs137852262
F9
1.000 0.080 X 139561865 missense variant A/G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 0
dbSNP: rs398122990
rs398122990
F9
1.000 0.080 X 139541073 splice region variant A/G snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 0
dbSNP: rs137852236
rs137852236
F9
1.000 0.080 X 139548467 missense variant A/G;T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 0
dbSNP: rs137852226
rs137852226
F9
1.000 0.080 X 139537139 missense variant A/T 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: rs137852245
rs137852245
F9
1.000 0.080 X 139551251 missense variant A/T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 0
dbSNP: rs137852270
rs137852270
F9
1.000 0.080 X 139562054 stop gained A/T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 0
dbSNP: rs587776736
rs587776736
F9
1.000 0.080 X 139551079 frameshift variant AG/- delins
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 0
dbSNP: rs137852469
rs137852469
F8
0.925 0.080 X 154860588 missense variant C/A snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019
dbSNP: rs549591993
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2015 2015
dbSNP: rs773084111
rs773084111
AK3
1.000 0.080 9 4713088 missense variant C/A snv 8.0E-06 7.0E-06
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.010 1.000 1 2011 2011
dbSNP: rs137852360
rs137852360
F8
0.925 0.080 X 154837676 missense variant C/A;G;T snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B
0.700 1.000 1 2019 2019