{{Rsnum
|rsid=12413409
|Gene=CNNM2
|Chromosome=10
|position=104719096
|Orientation=plus
|GMAF=0.1382
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 13.3 | 85.8
| HCB | 9.5 | 40.1 | 50.4
| JPT | 7.1 | 39.8 | 53.1
| YRI | 0.0 | 4.8 | 95.2
| ASW | 0.0 | 8.8 | 91.2
| CHB | 9.5 | 40.1 | 50.4
| CHD | 8.3 | 42.2 | 49.5
| GIH | 5.9 | 38.6 | 55.4
| LWK | 0.0 | 6.4 | 93.6
| MEX | 6.9 | 27.6 | 65.5
| MKK | 0.0 | 8.3 | 91.7
| TSI | 0.0 | 22.5 | 77.5
| HapMapRevision=28
}}

Based on a large study (~6,000 cases and 14,000 controls) of both European and Japanese populations, the [[rs12413409]](G) allele has been associated with higher risk of [[aneurysm]], with an odds ratio per allele of 1.29 (CI:1.19-1.40, p=1.2e-09). {{PMID|20364137|OA=1
}}

Also: [http://blog.23andme.com/2009/05/12/snpwatch-researchers-find-more-genetic-variations-associated-with-blood-pressure/ 23andMe blog] [[blood pressure]]

{{omim
|id=105800
|rsnum=12413409
}}

{{PMID Auto GWAS
|PMID=21378990
|Trait=None
|Title=Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
|RiskAllele=G
|Pval=1E-9
|OR=1.1200
|ORtxt=[1.08-1.16]
|OA=1
}}

{{PMID Auto GWAS
|PMID=21378988
|Trait=None
|Title=A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease
|RiskAllele=
|Pval=0.000004
|OR=None
|ORtxt=None
}}

[[Coronary Heart Disease]]

[[High Blood Pressure (Hypertension)]]

{{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=A
  |Pval=1E-6
  |OR=1.12
  |ORtxt=[1.08-1.19]
  }}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}