{{Rsnum
|rsid=387907135
|Chromosome=11
|position=61368609
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TMEM138
|Gene_s=TMEM138
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=11
|CLNACC=RCV000024190.1
|CLNALLE=1
|CLNDBN=Joubert syndrome 16
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1325:C3280906:614465:2318
|CLNHGVS=NC_000011.9:g.61136081A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614459.0005
|Disease=Joubert syndrome 16
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=61136081
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907135
|GENEINFO=TMEM138:51524
|GENE_ID=51524
|GENE_NAME=TMEM138
}}