rs772061412, 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 A
CUI: C0019069
Disease: Hemophilia A
295 0.925 0.080 X 139561664 missense variant C/G snv 5.5E-06 0.010 1.000 1 2011 2011
Mild hereditary factor VIII deficiency disease
CUI: C0272324
Disease: Mild hereditary factor VIII deficiency disease
6 0.925 0.080 X 139561664 missense variant C/G snv 5.5E-06 0.010 1.000 1 2011 2011