{{Rsnum
|rsid=200799769
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TMEM231
|position=75542641
|Gene_s=TMEM231
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=16
|CLNACC=RCV000033042.1
|CLNALLE=1
|CLNDBN=Joubert syndrome 20
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=CN162975:614970:220493:475
|CLNHGVS=NC_000016.9:g.75576539C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614949.0002
|Disease=Joubert syndrome 20
|FwdALT=T
|FwdREF=C
|GENEINFO=TMEM231:79583
|GENE_ID=79583
|GENE_NAME=TMEM231
|REF=C
|RSPOS=75576539
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=200799769
}}