{{Rsnum
|rsid=397514609
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=TMEM231
|position=75556198
|Gene_s=TMEM231
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=16
|CLNACC=RCV000033041.1
|CLNALLE=1
|CLNDBN=Joubert syndrome 20
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=CN162975:614970:220493:475
|CLNHGVS=NC_000016.9:g.75590096A>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614949.0001
|Disease=Joubert syndrome 20
|FwdALT=A
|FwdREF=T
|GENEINFO=TMEM231:79583
|GENE_ID=79583
|GENE_NAME=TMEM231
|REF=A
|RSPOS=75590096
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514609
}}