{{Rsnum
|rsid=6716724
|Gene=LOC650157
|Chromosome=2
|position=11370822
|Orientation=plus
|GMAF=0.2273
|Gene_s=RPL12
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 2.7 | 23.0 | 74.3
| HCB | 10.9 | 36.5 | 52.6
| JPT | 10.7 | 47.3 | 42.0
| YRI | 9.5 | 38.1 | 52.4
| ASW | 5.4 | 46.4 | 48.2
| CHB | 10.9 | 36.5 | 52.6
| CHD | 18.3 | 45.9 | 35.8
| GIH | 12.0 | 44.0 | 44.0
| LWK | 2.7 | 40.9 | 56.4
| MEX | 1.8 | 24.6 | 73.7
| MKK | 4.0 | 31.8 | 64.2
| TSI | 7.9 | 33.7 | 58.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21658281
|Trait=None
|Title=GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.
|RiskAllele=
|Pval=6E-7
|OR=1.3900
|ORtxt=[1.22-1.57]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}