{{Rsnum
|rsid=199821258
|Gene=TMEM67
|Chromosome=8
|position=93765648
|Orientation=plus
|GMAF=0.0004591
|Gene_s=TMEM67
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ClinVar
|ALT=G
|CAF=0.9995; 0.0004591
|CHROM=8
|CLNACC=RCV000050199.1
|CLNALLE=1
|CLNDBN=Meckel syndrome type 3
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1846357:607361:564
|CLNHGVS=NC_000008.10:g.94777876T>G
|CLNSIG=4
|COMMON=0
|Disease=Meckel syndrome type 3
|FwdALT=G
|FwdREF=T
|GENEINFO=TMEM67:91147
|GENE_ID=91147
|GENE_NAME=TMEM67
|REF=T
|RSPOS=94777876
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000016110100
|WGT=0
|dbSNPBuildID=137
|rsid=199821258
}}{{PMID Auto
|PMID=17397051
|Title=Spectrum of MKS1 and MKS3 mutations in Meckel syndrome: a genotype-phenotype correlation. Mutation in brief #960. Online.
}}