{{Rsnum
|rsid=397514754
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=TMEM231
|position=75540130
|Gene_s=TMEM231
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=16
|CLNACC=RCV000054807.1
|CLNALLE=1
|CLNDBN=Meckel syndrome, type 11
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN179854:615397:564
|CLNHGVS=NC_000016.9:g.75574028T>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614949.0004
|Disease=Meckel syndrome
|FwdALT=C
|FwdREF=A
|GENEINFO=TMEM231:79583
|GENE_ID=79583
|GENE_NAME=TMEM231
|REF=T
|RSPOS=75574028
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514754
}}