{{Rsnum
|rsid=111619594
|Gene=TMEM67
|Chromosome=8
|position=93780962
|Orientation=plus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=TMEM67
}}{{omim
|id=609884
|rsnum=111619594
|variant=0012
}}{{ClinVar
|rsid=111619594
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=94793190
|CHROM=8
|GMAF=0.0014
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x05016000000004011e110100
|GENEINFO=TMEM67:91147
|GENE_NAME=TMEM67
|GENE_ID=91147
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.94793190A>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;SLO;VLD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNACC=RCV000001444.1
|CLNDBN=Bardet-Biedl syndrome 14, modifier of
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=609884.0012
|COMMON=1
|Disease=Bardet-Biedl syndrome 14
}}