{{Rsnum
|rsid=4544423
|Gene=MEIS1
|Chromosome=2
|position=66522885
|Orientation=plus
|GMAF=0.4238
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=MEIS1
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 30.9 | 47.3 | 21.8
| HCB | 65.4 | 30.9 | 3.7
| JPT | 52.3 | 34.9 | 12.8
| YRI | 6.1 | 34.7 | 59.2
| ASW | 8.8 | 43.9 | 47.4
| CHB | 65.4 | 30.9 | 3.7
| CHD | 60.6 | 33.9 | 5.5
| GIH | 53.5 | 40.6 | 5.9
| LWK | 5.5 | 38.5 | 56.0
| MEX | 45.6 | 43.9 | 10.5
| MKK | 2.6 | 38.5 | 59.0
| TSI | 38.2 | 54.9 | 6.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=19223043
|Title=Exploring the genetic link between RLS and [[ADHD]]
}}

{{PMID Auto
|PMID=19126776
|Title=MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels.
|OA=1
}}

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