{{Rsnum
|rsid=199469707
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TMEM237
|position=201640915
|Gene_s=TMEM237
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199469707
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=202505638
|CHROM=2
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.202505638G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1325; 614423.0001
|CLNSIG=5
|CLNCUI=CN120487
|CLNDBN=Joubert syndrome 14; Familial aplasia of the vermis
|Disease=Joubert syndrome 14; Familial aplasia of the vermis
|CLNACC=RCV000024179.1; RCV000034999.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:Orphanet:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1325:C3280766:614424:220493:220497:2318:475; NBK1325:C0431399:213300:475:253175003
|GENEINFO=TMEM237:65062
|GENE_ID=65062
|GENE_NAME=TMEM237
}}{{PMID Auto
|PMID=17603801
|Title=Meckel syndrome in the Hutterite population is actually a Joubert-related cerebello-oculo-renal syndrome.
}}{{PMID Auto
|PMID=22152675
|Title=TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone.
|OA=1
}}