{{Rsnum
|rsid=6710341
|Gene=MEIS1
|Chromosome=2
|position=66531290
|Orientation=plus
|GMAF=0.1915
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MEIS1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 70.5 | 25.9 | 3.6
| HCB | 55.5 | 40.9 | 3.6
| JPT | 54.9 | 42.5 | 2.7
| YRI | 70.7 | 27.2 | 2.0
| ASW | 56.1 | 42.1 | 1.8
| CHB | 55.5 | 40.9 | 3.6
| CHD | 52.3 | 39.4 | 8.3
| GIH | 44.6 | 42.6 | 12.9
| LWK | 68.2 | 30.0 | 1.8
| MEX | 65.5 | 31.0 | 3.4
| MKK | 60.9 | 33.3 | 5.8
| TSI | 61.8 | 36.3 | 2.0
| HapMapRevision=28
}}
[[rs6710341]], a SNP located in the [[MEIS1]] gene, has been linked to [[restless legs syndrome]], a common sleep disorder, with an overall odds ratio of 0.96 (CI: 0.77-1.17) for the (G) risk allele. {{PMID|17637780}}

The association from this region that gives the highest association to [[restless legs syndrome]], however, is a haplotype consisting of the [[rs6710341(A)]] and [[rs12469063(G)]] alleles. This haplotype gives rise to an odds ratio of 2.75 (CI: 2.23-3.41). {{PMID|17637780}}

{{PMID Auto
|PMID=19223043
|Title=Exploring the genetic link between RLS and [[ADHD]]
}}

{{PMID Auto
|PMID=19279021
|Title=Replication of restless legs syndrome loci in three European populations.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}