{{Rsnum
|rsid=736707
|Gene=RELN
|Chromosome=7
|position=103489956
|Orientation=minus
|GMAF=0.3407
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=LOC101927870,RELN
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 3.5 | 45.1 | 51.3
| HCB | 20.6 | 48.5 | 30.9
| JPT | 26.5 | 57.5 | 15.9
| YRI | 24.7 | 52.7 | 22.6
| ASW | 24.6 | 54.4 | 21.1
| CHB | 20.6 | 48.5 | 30.9
| CHD | 19.3 | 47.7 | 33.0
| GIH | 9.9 | 55.4 | 34.7
| LWK | 15.6 | 56.9 | 27.5
| MEX | 5.2 | 15.5 | 79.3
| MKK | 16.7 | 53.2 | 30.1
| TSI | 6.9 | 28.4 | 64.7
| 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=18597938
|Title=Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population.
}}

{{PMID Auto
|PMID=23216241
|Title=Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.
|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}}