{{Rsnum
|rsid=397514753
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TMEM231
|position=75542602
|Gene_s=TMEM231
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=16
|CLNACC=RCV000054806.1
|CLNALLE=1
|CLNDBN=Meckel syndrome, type 11
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN179854:615397:564
|CLNHGVS=NC_000016.9:g.75576500C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614949.0003
|Disease=Meckel syndrome
|FwdALT=A
|FwdREF=G
|GENEINFO=TMEM231:79583
|GENE_ID=79583
|GENE_NAME=TMEM231
|REF=C
|RSPOS=75576500
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514753
}}