{{Rsnum
|rsid=201884120
|Chromosome=18
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RTTN
|position=70205267
|Gene_s=RTTN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=18
|CLNACC=RCV000030786.1; RCV000059811.1
|CLNALLE=1
|CLNDBN=Polymicrogyria with seizures; not provided
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN143955:614833
|CLNHGVS=NC_000018.9:g.67872503C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=610436.0002; VAR_069094
|Disease=Polymicrogyria with seizures; not provided
|FwdALT=T
|FwdREF=C
|GENEINFO=RTTN:25914
|GENE_ID=25914
|GENE_NAME=RTTN
|REF=C
|RSPOS=67872503
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050168000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=201884120
}}{{PMID Auto
|PMID=22939636
|Title=RTTN mutations link primary cilia function to organization of the human cerebral cortex.
|OA=1
}}