{{Rsnum
|rsid=2207418
|Chromosome=20
|position=11194255
|Orientation=minus
|GMAF=0.3609
|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 | 8.8 | 37.2 | 54.0
| HCB | 42.3 | 42.3 | 15.3
| JPT | 34.5 | 44.2 | 21.2
| YRI | 6.1 | 27.2 | 66.7
| ASW | 1.8 | 36.8 | 61.4
| CHB | 42.3 | 42.3 | 15.3
| CHD | 37.6 | 51.4 | 11.0
| GIH | 8.9 | 39.6 | 51.5
| LWK | 0.9 | 20.2 | 78.9
| MEX | 27.6 | 41.4 | 31.0
| MKK | 1.3 | 14.1 | 84.6
| TSI | 6.9 | 37.3 | 55.9
| HapMapRevision=28
}}[[rs2207418]] is a SNP located in a 'gene desert' region of ch 20p12.

In an Amish founder population of 851 individuals, the [[rs2207418]](C) allele was associated with cardiac hypertrophy, increased risk of [[heart failure]] (relative risk 1.85, CI: 1.2 - 2.7, p = 0.0019), and increased mortality (hazard risk 1.5, CI: 1.2 - 1.9, p = 0.0004).{{PMID|21348951}}

{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}