{{Rsnum
|rsid=12410279
|Chromosome=1
|position=220678178
|Orientation=plus
|GMAF=0.2112
|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 | 76.1 | 22.1 | 1.8
| HCB | 35.0 | 49.6 | 15.3
| JPT | 30.1 | 47.8 | 22.1
| YRI | 100.0 | 0.0 | 0.0
| ASW | 93.0 | 7.0 | 0.0
| CHB | 35.0 | 49.6 | 15.3
| CHD | 38.5 | 50.5 | 11.0
| GIH | 60.4 | 34.7 | 5.0
| LWK | 94.5 | 5.5 | 0.0
| MEX | 43.1 | 43.1 | 13.8
| MKK | 89.1 | 10.9 | 0.0
| TSI | 71.6 | 27.5 | 1.0
| HapMapRevision=28
}}{{PMID|18492799}} Haplotype [[rs12740310]]*C-[[rs3737296]]*G-[[rs12410279]]*A was overtransmitted (p(corrected)=0.0016), with a relative risk for [[autism]] of 1.8 in homozygous carriers

{{omim
|desc=MAP/MICROTUBULE AFFINITY-REGULATING KINASE 1; MARK1
|id=606511
|rsnum=12410279
}}

{{omim
|id=610836
|rsnum=12410279
}}

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