{{Rsnum
|rsid=2592394
|Chromosome=2
|position=176127051
|Orientation=minus
|GMAF=0.3448
|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 | 47.8 | 42.5 | 9.7
| HCB | 19.0 | 46.0 | 35.0
| JPT | 20.4 | 52.2 | 27.4
| YRI | 70.1 | 26.5 | 3.4
| ASW | 75.4 | 22.8 | 1.8
| CHB | 19.0 | 46.0 | 35.0
| CHD | 17.4 | 46.8 | 35.8
| GIH | 51.5 | 38.6 | 9.9
| LWK | 54.5 | 39.1 | 6.4
| MEX | 63.8 | 27.6 | 8.6
| MKK | 61.5 | 35.3 | 3.2
| TSI | 46.1 | 44.1 | 9.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20700443
|Trait=None
|Title=Genome-Wide Association Studies of Serum Magnesium, Potassium, and Sodium Concentrations Identify Six Loci Influencing Serum Magnesium Levels
|RiskAllele=A
|Pval=5E-7
|OR=0
|ORtxt=[0.002-0.006] mmol/L decrease
|OA=1
}}

{{PMID|19938081|OA=1
}} Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}