rs137852247, 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 0.925 0.080 X 139560852 missense variant G/A snv 0.800 0
Abnormality of coagulation
CUI: C1846821
Disease: Abnormality of coagulation
15 0.925 0.080 X 139560852 missense variant G/A snv 0.700 1.000 1 2019 2019
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
295 0.925 0.080 X 139560852 missense variant G/A snv 0.700 1.000 1 2019 2019