{{Rsnum
|rsid=39335
|Gene=RELN
|Chromosome=7
|position=103813122
|Orientation=minus
|GMAF=0.1676
|Gene_s=RELN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 75.2 | 22.1 | 2.7
| HCB | 85.4 | 14.6 | 0.0
| JPT | 90.3 | 9.7 | 0.0
| YRI | 38.1 | 51.0 | 10.9
| ASW | 47.4 | 47.4 | 5.3
| CHB | 85.4 | 14.6 | 0.0
| CHD | 89.9 | 10.1 | 0.0
| GIH | 74.3 | 23.8 | 2.0
| LWK | 59.1 | 38.2 | 2.7
| MEX | 63.8 | 31.0 | 5.2
| MKK | 59.6 | 34.0 | 6.4
| TSI | 73.5 | 25.5 | 1.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=24227897
|Title=The rs39335 polymorphism of the RELN gene is not associated with otosclerosis in a southern Italian population
|OA=1
}}

{{PMID Auto
|PMID=19230858
|Title=A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.
|OA=1
}}

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