rs137852259, F9

N. diseases: 2
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 139561821 missense variant G/A snv 0.800 1.000 2 2012 2013
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
295 0.925 0.080 X 139561821 missense variant G/A snv 0.700 1.000 1 2019 2019