{{Rsnum
|rsid=11230683
|Gene=TMEM216
|Chromosome=11
|position=61397797
|Orientation=plus
|GMAF=0.003673
|Gene_s=TMEM216
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ClinVar
|ALT=A,T
|CAF=0.9963; 0.003673; .
|CHROM=11
|CLNACC=RCV000049797.1
|CLNALLE=2
|CLNDBN=Meckel syndrome type 2
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1864148:603194:564
|CLNHGVS=NC_000011.9:g.61165269C>T
|CLNSIG=4
|COMMON=1
|Disease=Meckel syndrome type 2
|FwdALT=A,T
|FwdREF=C
|GENEINFO=TMEM216:51259
|GENE_ID=51259
|GENE_NAME=TMEM216
|REF=C
|RSPOS=61165269
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000416110100
|WGT=0
|dbSNPBuildID=120
|rsid=11230683
}}{{PMID Auto
|PMID=20512146
|Title=Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes.
|OA=1
}}