rs111033613, 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 0.925 0.080 X 154928668 missense variant G/A;T snv 0.800 1.000 22 1989 2013
FACTOR VIII (EAST HARTFORD) PHENOTYPE
CUI: C4017565
Disease: FACTOR VIII (EAST HARTFORD) PHENOTYPE
1 0.925 0.080 X 154928668 missense variant G/A;T snv 0.700 0
Severe hereditary factor VIII deficiency disease
CUI: C0272322
Disease: Severe hereditary factor VIII deficiency disease
15 0.925 0.080 X 154928668 missense variant G/A;T snv 0.010 1.000 1 1996 1996