{{Rsnum
|rsid=137853108
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=TMEM67
|position=93765617
|Gene_s=TMEM67
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=609884
|variant=0011
|rsnum=137853108
}}{{ClinVar
|rsid=137853108
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=94777845
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000040002110100
|GENEINFO=TMEM67:91147
|GENE_NAME=TMEM67
|GENE_ID=91147
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.94777845A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609884.0011
|CLNSIG=5
|CLNCUI=C1846357; C1853153
|CLNDBN=Meckel syndrome type 3; Joubert syndrome 6
|Disease=Meckel syndrome type 3; Joubert syndrome 6
|CLNACC=RCV000001442.1; RCV000001443.1
|Tags=PM;VLD;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C1846357:607361:564; NBK1325:C1853153:610688:475
}}