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: rs626035
rs626035
ABO
9 133259603 intron variant T/G snv 0.28
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs626035
rs626035
ABO
9 133259603 intron variant T/G snv 0.28
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0.700 1.000 1 2013 2013
dbSNP: rs626035
rs626035
ABO
9 133259603 intron variant T/G snv 0.28
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs626035
rs626035
ABO
9 133259603 intron variant T/G snv 0.28
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2011 2011
dbSNP: rs672316
rs672316
ABO
9 133262722 intron variant T/G snv 0.29
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2011 2011
dbSNP: rs672316
rs672316
ABO
9 133262722 intron variant T/G snv 0.29
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0.700 1.000 1 2013 2013
dbSNP: rs672316
rs672316
ABO
9 133262722 intron variant T/G snv 0.29
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs58081338
rs58081338
ABO
9 133252942 non coding transcript exon variant T/C;G snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs673578
rs673578
ABO
9 133262454 intron variant T/C;G snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs7873635
rs7873635
ABO
9 133256625 intron variant T/C;G snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs10901253
rs10901253
ABO
9 133253385 non coding transcript exon variant T/C snv 0.27
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs1633513
rs1633513
ABO
9 133265051 intron variant T/C snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs1752339
rs1752339
ABO
9 133265724 intron variant T/C snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs2519093
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.820 1.000 1 2011 2019
dbSNP: rs2519093
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs475419
rs475419
ABO
9 133272816 intron variant T/C snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs494242
rs494242
ABO
9 133269706 intron variant T/C snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs547495
rs547495
ABO
9 133259604 intron variant T/C snv 0.28
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs574347
rs574347
ABO
9 133260255 intron variant T/C snv 0.27
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0.700 1.000 1 2013 2013
dbSNP: rs574347
rs574347
ABO
9 133260255 intron variant T/C snv 0.27
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2011 2011
dbSNP: rs574347
rs574347
ABO
9 133260255 intron variant T/C snv 0.27
CUI: C0202202
Disease: Protein measurement
Protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs581107
rs581107
ABO
9 133272287 intron variant T/C snv
CUI: C0042487
Disease: Venous Thrombosis
Venous Thrombosis 		0.700 1.000 1 2012 2012
dbSNP: rs77641731
rs77641731
ABO
1.000 0.040 9 133257521 missense variant T/C snv
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs77641731
rs77641731
ABO
1.000 0.040 9 133257521 missense variant T/C snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		0.700 1.000 1 2012 2012
dbSNP: rs77641731
rs77641731
ABO
1.000 0.040 9 133257521 missense variant T/C snv
CUI: C0024530
Disease: Malaria
Malaria 		0.700 1.000 1 2012 2012