{{Rsnum
|rsid=137853107
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TMEM67
|position=93791282
|Gene_s=TMEM67
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=609884
|variant=0006
|rsnum=137853107
}}{{ClinVar
|rsid=137853107
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=94803510
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=TMEM67:91147
|GENE_NAME=TMEM67
|GENE_ID=91147
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.94803510A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609884.0006
|CLNSIG=5
|CLNCUI=C1853153; C1857662
|CLNDBN=Joubert syndrome 6; COACH syndrome
|Disease=Joubert syndrome 6; COACH syndrome
|CLNACC=RCV000001436.2; RCV000001437.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1325:C1853153:610688:475; C1857662:216360:1454
}}