{{Rsnum
|rsid=387907131
|Chromosome=2
|position=201640264
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TMEM237
|Gene_s=TMEM237
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=2
|CLNACC=RCV000024182.1
|CLNALLE=1
|CLNDBN=Joubert syndrome 14
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:Orphanet:Orphanet
|CLNDSDBID=NBK1325:C3280766:614424:220493:220497:2318:475
|CLNHGVS=NC_000002.11:g.202504987G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614423.0004
|Disease=Joubert syndrome 14
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=202504987
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907131
|GENEINFO=TMEM237:65062
|GENE_ID=65062
|GENE_NAME=TMEM237
}}