{{Rsnum
|rsid=1105434
|Gene=REST
|Chromosome=4
|position=56927585
|Orientation=plus
|GMAF=0.3122
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=REST
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 15.9 | 53.1 | 31.0
| HCB | 8.8 | 39.0 | 52.2
| JPT | 6.2 | 31.2 | 62.5
| YRI | 2.0 | 32.7 | 65.3
| ASW | 5.3 | 33.3 | 61.4
| CHB | 8.8 | 39.0 | 52.2
| CHD | 5.5 | 28.4 | 66.1
| GIH | 5.9 | 32.7 | 61.4
| LWK | 5.6 | 27.8 | 66.7
| MEX | 31.0 | 46.6 | 22.4
| MKK | 4.5 | 26.3 | 69.2
| TSI | 10.8 | 48.0 | 41.2
| HapMapRevision=28
}}

{{omim
|desc=KAHRIZI SYNDROME
|id=612713
|rsnum=1105434
}}

{{PMID Auto
|PMID=18781183
|Title=An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4.
|OA=1
}}

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