{{Rsnum
|rsid=2229864
|Gene=RELN
|Chromosome=7
|position=103515258
|Orientation=minus
|GMAF=0.4256
|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 | 9.8 | 50.0 | 40.2
| HCB | 61.0 | 36.0 | 2.9
| JPT | 60.2 | 37.2 | 2.7
| YRI | 74.1 | 23.8 | 2.0
| ASW | 56.1 | 35.1 | 8.8
| CHB | 61.0 | 36.0 | 2.9
| CHD | 67.0 | 31.2 | 1.8
| GIH | 35.6 | 46.5 | 17.8
| LWK | 61.1 | 32.4 | 6.5
| MEX | 13.8 | 36.2 | 50.0
| MKK | 50.0 | 41.7 | 8.3
| TSI | 18.6 | 46.1 | 35.3
| 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
}}

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