Source: GWASDB

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: rs630014
rs630014
ABO
9 133274306 intron variant G/A;C snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 2 2011 2012
dbSNP: rs630014
rs630014
ABO
9 133274306 intron variant G/A;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: rs630014
rs630014
ABO
9 133274306 intron variant G/A;C snv
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs630014
rs630014
ABO
9 133274306 intron variant G/A;C snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs630014
rs630014
ABO
9 133274306 intron variant G/A;C snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs630014
rs630014
ABO
9 133274306 intron variant G/A;C snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs630014
rs630014
ABO
9 133274306 intron variant G/A;C snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs630014
rs630014
ABO
9 133274306 intron variant G/A;C snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs630014
rs630014
ABO
9 133274306 intron variant G/A;C snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012