Source: GWASCAT

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: rs505922
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.720 1.000 1 2013 2018
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: rs505922
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		0.700 1.000 1 2017 2017
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: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.710 1.000 1 2018 2019
dbSNP: rs507666
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs507666
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv
CUI: C4722217
Disease: E-selectin Measurement
E-selectin Measurement 		0.700 1.000 1 2017 2017
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: rs514659
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2011 2011
dbSNP: rs529565
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv
CUI: C0034065
Disease: Pulmonary Embolism
Pulmonary Embolism 		0.700 1.000 1 2016 2016
dbSNP: rs529565
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv
CUI: C0149871
Disease: Deep Vein Thrombosis
Deep Vein Thrombosis 		0.700 1.000 1 2016 2016
dbSNP: rs529565
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.700 1.000 1 2016 2016
dbSNP: rs529565
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.720 0.667 1 2016 2018
dbSNP: rs532436
rs532436
ABO
1.000 0.080 9 133274414 intron variant A/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs532436
rs532436
ABO
1.000 0.080 9 133274414 intron variant A/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2015 2015
dbSNP: rs550057
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs550057
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs550057
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2019 2019
dbSNP: rs550057
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs550057
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs582094
rs582094
ABO
9 133270074 intron variant T/A snv
CUI: C4317009
Disease: Diverticular Diseases
Diverticular Diseases 		0.700 1.000 1 2018 2018
dbSNP: rs587611953
rs587611953
ABO
9 133270004 intron variant C/A snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs587729126
rs587729126
ABO
9 133263363 intron variant CACCACTACGCC/- delins
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
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: rs62641786
rs62641786
ABO
9 133255290 3 prime UTR variant T/C;G snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0.700 1.000 1 2019 2019