rs61754011, VWF

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.
von Willebrand Disease, Type 2
CUI: C1264040
Disease: von Willebrand Disease, Type 2
39 0.882 0.160 12 6057930 missense variant C/T snv 0.700 0
von Willebrand Disease, Type 2A
CUI: C1282968
Disease: von Willebrand Disease, Type 2A
17 0.882 0.160 12 6057930 missense variant C/T snv 0.700 0
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.882 0.160 12 6057930 missense variant C/T snv 0.010 1.000 1 2006 2006