{{Rsnum
|rsid=137853106
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=TMEM67
|position=93782456
|Gene_s=TMEM67
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=609884
|variant=0004
|rsnum=137853106
}}{{ClinVar
|rsid=137853106
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=94794684
|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.94794684A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=609884.0004
|CLNSIG=5
|CLNCUI=C1846357
|CLNDBN=Meckel syndrome type 3
|Disease=Meckel syndrome type 3
|CLNACC=RCV000001434.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1846357:607361:564
}}