rs2519093, ABO

N. diseases: 16
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.882 0.200 9 133266456 intron variant T/C snv 0.820 1.000 4 2011 2019
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 2 2015 2018
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 2 2018 2018
Alkaline phosphatase measurement
CUI: C0201850
Disease: Alkaline phosphatase measurement
79 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2018 2018
Allergic Reaction
CUI: C1527304
Disease: Allergic Reaction
1019 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2016 2016
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2018 2018
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2018 2018
E-selectin Measurement
CUI: C4722217
Disease: E-selectin Measurement
6 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2019 2019
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2019 2019
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2018 2018
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2018 2018
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2018 2018
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2018 2018
Venous Thrombosis
CUI: C0042487
Disease: Venous Thrombosis
218 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2012 2012
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 0.882 0.200 9 133266456 intron variant T/C snv 0.700 1.000 1 2019 2019
Paroxysmal nocturnal hemoglobinuria
CUI: C0024790
Disease: Paroxysmal nocturnal hemoglobinuria
12 0.882 0.200 9 133266456 intron variant T/C snv 0.010 1.000 1 2017 2017