{{Rsnum
|rsid=3842936
|Chromosome=12
|position=58407244
|Orientation=plus
|GMAF=0.4729
|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 | 12.4 | 52.2 | 35.4
| HCB | 31.4 | 49.6 | 19.0
| JPT | 14.2 | 67.3 | 18.6
| YRI | 27.2 | 50.3 | 22.4
| ASW | 21.1 | 54.4 | 24.6
| CHB | 31.4 | 49.6 | 19.0
| CHD | 18.3 | 61.5 | 20.2
| GIH | 17.0 | 51.0 | 32.0
| LWK | 24.8 | 43.1 | 32.1
| MEX | 21.1 | 47.4 | 31.6
| MKK | 25.6 | 51.9 | 22.4
| TSI | 14.7 | 53.9 | 31.4
| HapMapRevision=28
}}{{omim
|desc=NATIVE AMERICAN MYOPATHY
|id=255995
|rsnum=3842936
}}

This SNP has been investigated in regard to a syndrome known as [[Native American myopathy]]. [http://omim.org/entry/255995 OMIM]

{{PMID Auto
|PMID=18843099
|Title=Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1.
}}

{{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}}