{{Rsnum
|rsid=884202
|Gene=MAP2K5
|Chromosome=15
|position=67762050
|Orientation=plus
|GMAF=0.4601
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MAP2K5
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 46.9 | 49.6 | 3.5
| HCB | 10.2 | 54.7 | 35.0
| JPT | 13.4 | 42.9 | 43.8
| YRI | 33.3 | 49.0 | 17.7
| ASW | 28.1 | 54.4 | 17.5
| CHB | 10.2 | 54.7 | 35.0
| CHD | 18.3 | 43.1 | 38.5
| GIH | 32.0 | 40.0 | 28.0
| LWK | 37.6 | 50.5 | 11.9
| MEX | 12.1 | 50.0 | 37.9
| MKK | 39.7 | 47.4 | 12.8
| TSI | 46.1 | 40.2 | 13.7
| HapMapRevision=28
}}[[rs884202]], a SNP located in a region of chromosome 15q, has been linked to a lower frequency of [[restless legs syndrome]], a common sleep disorder, with an overall odds ratio of 0.69 (CI: 0.58-0.81) for the (G) minor allele. {{PMID|17637780}}

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