{{Rsnum
|rsid=579459
|Chromosome=9
|position=133278724
|Orientation=plus
|GMAF=0.1887
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 2.7 | 35.4 | 61.9
| HCB | 3.6 | 25.5 | 70.8
| JPT | 1.8 | 43.4 | 54.9
| YRI | 1.4 | 24.5 | 74.1
| ASW | 3.5 | 19.3 | 77.2
| CHB | 3.6 | 25.5 | 70.8
| CHD | 2.8 | 27.5 | 69.7
| GIH | 2.0 | 23.8 | 74.3
| LWK | 3.6 | 22.7 | 73.6
| MEX | 3.4 | 19.0 | 77.6
| MKK | 1.9 | 17.9 | 80.1
| TSI | 10.8 | 28.4 | 60.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19729612
|Trait=Serum soluble E-selectin
|Title=Genome-Wide Association Identifies the ABO Blood Group as a Major Locus Associated With Serum Levels of Soluble E-Selectin
|RiskAllele=C
|Pval=1E-29
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID Auto GWAS
|PMID=20167578
|Trait=Soluble levels of adhesion molecules
|Title=Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels
|RiskAllele=T
|Pval=2E-41
|OR=14.00
|ORtxt=[12.04-15.96] % increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=21378990
|Trait=None
|Title=Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
|RiskAllele=C
|Pval=4E-14
|OR=1.1000
|ORtxt=[1.07-1.13]
|OA=1
}}

{{PMID Auto
|PMID=22010135
|Title=Association of Variation at the ABO Locus with Circulating Levels of sICAM-1, sP-selectin and sE-selectin: A Meta-Analysis
|OA=1
}}

{{PMID Auto GWAS
|PMID=22001757
|Trait=None
|Title=Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.
|RiskAllele=T
|Pval=3E-123
|OR=8.8000
|ORtxt=None
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs579459
|overall_frequency_n=18
|overall_frequency_d=128
|overall_frequency=0.140625
|n_genomes=12
|n_genomes_annotated=0
|n_haplomes=15
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

[[Coronary Heart Disease]]

{{PMID Auto GWAS
  |PMID=23222517
  |Trait=Red blood cell traits
  |Title=Seventy-five genetic loci influencing the human red blood cell.
  |RiskAllele=T
  |Pval=9E-18
  |OR=.02
  |ORtxt=[0.015-0.027] unit increase
  |OA=1
}}

{{PMID Auto
|PMID=23161703
|Title=Influence of 23 coronary artery disease variants on recurrent myocardial infarction or cardiac death: the GRACE Genetics Study.
}}

{{PMID Auto GWAS
  |PMID=24262325
  |Trait=Coronary artery disease
  |Title=Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
  |RiskAllele=C
  |Pval=2E-7
  |OR=1.10
  |ORtxt=[1.06-1.14]
  }}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}