{{Rsnum
|rsid=39395
|Gene=RELN
|Chromosome=7
|position=103849282
|Orientation=plus
|GMAF=0.4624
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=RELN
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 36.3 | 42.5 | 21.2
| HCB | 25.5 | 51.8 | 22.6
| JPT | 26.5 | 46.9 | 26.5
| YRI | 34.0 | 48.3 | 17.7
| ASW | 49.1 | 40.4 | 10.5
| CHB | 25.5 | 51.8 | 22.6
| CHD | 31.8 | 45.8 | 22.4
| GIH | 20.8 | 37.6 | 41.6
| LWK | 40.9 | 47.3 | 11.8
| MEX | 32.8 | 51.7 | 15.5
| MKK | 53.2 | 39.7 | 7.1
| TSI | 22.5 | 50.0 | 27.5
| HapMapRevision=28
}}

{{omim
|desc=OTOSCLEROSIS; OTSC1
|id=166800
|rsnum=39395
}}

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

{{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}}