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: rs8176719
rs8176719
ABO
0.925 0.120 9 133257521 frameshift variant -/C ins 0.37 0.35
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.830 1.000 1 2012 2019
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: rs505922
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv
CUI: C0013295
Disease: Duodenal Ulcer
Duodenal Ulcer
0.810 1.000 1 2012 2012
dbSNP: rs505922
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.800 1.000 3 2009 2012
dbSNP: rs687621
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.800 1.000 3 2011 2013
dbSNP: rs529565
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.800 1.000 2 2011 2016
dbSNP: rs687289
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.800 1.000 2 2011 2019
dbSNP: rs505922
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.800 1.000 1 2013 2017
dbSNP: rs505922
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.800 1.000 1 2013 2013
dbSNP: rs507666
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 1 2013 2019
dbSNP: rs514659
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.800 1.000 1 2013 2017
dbSNP: rs643434
rs643434
ABO
9 133266942 intron variant A/G;T snv
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement
0.800 1.000 1 2012 2018
dbSNP: rs643434
rs643434
ABO
9 133266942 intron variant A/G;T snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.800 1.000 1 2013 2013
dbSNP: rs644234
rs644234
ABO
9 133266804 intron variant G/T snv
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.800 1.000 1 2012 2012
dbSNP: rs657152
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv
Thyroid stimulating hormone measurement
0.800 1.000 1 2013 2013
dbSNP: rs687289
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.800 1.000 1 2013 2019
dbSNP: rs687621
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv
Activated Partial Thromboplastin Time measurement
0.800 1.000 1 2012 2012
dbSNP: rs687621
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.800 1.000 1 2010 2013
dbSNP: rs8176719
rs8176719
ABO
0.925 0.120 9 133257521 frameshift variant -/C ins 0.37 0.35
CUI: C0024530
Disease: Malaria
Malaria
0.800 1.000 1 2012 2012
dbSNP: rs8176722
rs8176722
ABO
1.000 0.040 9 133257367 intron variant C/A snv 0.13 0.12
CUI: C0024530
Disease: Malaria
Malaria
0.800 1.000 1 2013 2013
dbSNP: rs8176743
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.800 1.000 1 2013 2013
dbSNP: rs8176746
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 1 2010 2012
dbSNP: rs8176749
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 1 2012 2018
dbSNP: rs505922
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
0.740 1.000 1 2009 2015