{{Rsnum
|rsid=362719
|Gene=RELN
|Chromosome=7
|position=103545430
|Orientation=plus
|GMAF=0.3439
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=RELN
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 29.2 | 70.8
| HCB | 12.6 | 45.9 | 41.5
| JPT | 8.9 | 43.8 | 47.3
| YRI | 59.2 | 35.4 | 5.4
| ASW | 47.4 | 36.8 | 15.8
| CHB | 12.6 | 45.9 | 41.5
| CHD | 13.1 | 49.5 | 37.4
| GIH | 12.9 | 45.5 | 41.6
| LWK | 37.3 | 44.5 | 18.2
| MEX | 5.2 | 31.0 | 63.8
| MKK | 25.8 | 45.8 | 28.4
| TSI | 1.0 | 32.4 | 66.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=21863557
|Title=A new single-nucleotide mutation (rs362719) of the reelin (RELN) gene associated with schizophrenia in female Chinese Han
}}

{{PMID Auto
|PMID=18597938
|Title=Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.
}}

{{PMID Auto
|PMID=19691043
|Title=Sex-specific association of the Reelin gene with bipolar disorder.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}