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: rs687289
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.700 1.000 1 2014 2014
dbSNP: rs8176743
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2014 2014
dbSNP: rs116552240
rs116552240
ABO
9 133273682 intron variant A/T snv
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		0.700 1.000 1 2015 2015
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: 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: rs10901252
rs10901252
ABO
9 133252613 non coding transcript exon variant G/C snv 0.11
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs10901252
rs10901252
ABO
9 133252613 non coding transcript exon variant G/C snv 0.11
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs149037075
rs149037075
ABO
9 133255469 3 prime UTR variant CTGT/- delins 0.15
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs149037075
rs149037075
ABO
9 133255469 3 prime UTR variant CTGT/- delins 0.15
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs2519093
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2016 2016
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: rs687289
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs687289
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		0.700 1.000 1 2016 2016
dbSNP: rs687621
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs8176643
rs8176643
ABO
9 133274294 intron variant C/- del
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs8176643
rs8176643
ABO
9 133274294 intron variant C/- del
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs8176644
rs8176644
ABO
9 133273734 intron variant C/T snv
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016
dbSNP: rs8176671
rs8176671
ABO
9 133266900 intron variant A/C snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs8176671
rs8176671
ABO
9 133266900 intron variant A/C snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs8176685
rs8176685
ABO
9 133263363 intron variant CACCACTACGCC/- delins
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs8176685
rs8176685
ABO
9 133263363 intron variant CACCACTACGCC/- delins
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs8176685
rs8176685
ABO
9 133263363 intron variant CACCACTACGCC/- delins
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs8176704
rs8176704
ABO
0.925 0.080 9 133260148 intron variant G/A snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0.700 1.000 1 2016 2016