Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs61750610
rs61750610
VWF
0.925 0.080 12 6013630 missense variant G/T snv
CUI: C0042974
Disease: von Willebrand Disease
von Willebrand Disease 		0.010 1.000 1 2006 2006
dbSNP: rs61750610
rs61750610
VWF
0.925 0.080 12 6013630 missense variant G/T snv
CUI: C2930849
Disease: Von willebrand factor, deficiency
Von willebrand factor, deficiency 		0.010 1.000 1 2006 2006
dbSNP: rs61750610
rs61750610
VWF
0.925 0.080 12 6013630 missense variant G/T snv
CUI: C0005779
Disease: Blood Coagulation Disorders
Blood Coagulation Disorders 		0.010 1.000 1 2006 2006