rs137852358, F8

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 A
CUI: C0019069
Disease: Hemophilia A
295 0.882 0.080 X 154861758 missense variant C/A;T snv 0.810 1.000 3 2010 2013
Hemophilia B
CUI: C0008533
Disease: Hemophilia B
125 0.882 0.080 X 154861758 missense variant C/A;T snv 0.700 1.000 1 2019 2019
Severe hereditary factor VIII deficiency disease
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
15 0.882 0.080 X 154861758 missense variant C/A;T snv 0.010 1.000 1 1996 1996