rs137852254, F9

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hemophilia B
CUI: C0008533
Disease: Hemophilia B
125 0.882 0.080 X 139561710 missense variant C/T snv 0.800 1.000 3 1991 2012
Thrombophilia, X-Linked, Due To Factor Ix Defect
CUI: C2749016
Disease: Thrombophilia, X-Linked, Due To Factor Ix Defect
5 0.882 0.080 X 139561710 missense variant C/T snv 0.700 1.000 3 1991 2012
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
295 0.882 0.080 X 139561710 missense variant C/T snv 0.700 1.000 1 2019 2019