{{Rsnum
|rsid=2073559
|Gene=RELN
|Chromosome=7
|position=103678477
|Orientation=plus
|GMAF=0.472
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=RELN
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 23.0 | 48.7 | 28.3
| HCB | 30.7 | 50.4 | 19.0
| JPT | 19.5 | 51.3 | 29.2
| YRI | 8.8 | 49.7 | 41.5
| ASW | 14.0 | 43.9 | 42.1
| CHB | 30.7 | 50.4 | 19.0
| CHD | 32.1 | 47.7 | 20.2
| GIH | 20.8 | 49.5 | 29.7
| LWK | 10.9 | 49.1 | 40.0
| MEX | 27.6 | 50.0 | 22.4
| MKK | 19.9 | 37.2 | 42.9
| TSI | 20.6 | 51.0 | 28.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=20554015
|Title=No significant association between RELN polymorphism and autism in case-control and family-based association study in Chinese Han population
}}

{{PMID Auto
|PMID=17621165
|Title=Investigation of potential gene-gene interactions between APOE and RELN contributing to autism risk.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}