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: rs2073827
rs2073827
ABO
9 133261730 intron variant G/C snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2011 2011
dbSNP: rs2073827
rs2073827
ABO
9 133261730 intron variant G/C snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0.700 1.000 1 2013 2013
dbSNP: rs2073827
rs2073827
ABO
9 133261730 intron variant G/C snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012