{{Rsnum
|rsid=63750743
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TMEM43
|position=14141665
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TMEM43
}}{{omim
|id=612048
|rsnum=63750743
|variant=0001
}}

{{ClinVar
|rsid=63750743
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=14183165
|CHROM=3
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=TMEM43:79188
|GENE_NAME=TMEM43
|GENE_ID=79188
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.14183165C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612048.0001
|CLNSIG=5
|CLNCUI=C1858379
|CLNDBN=Arrhythmogenic right ventricular cardiomyopathy, type 5; Arrhythmogenic right ventricular cardiomyopathy
|Disease=Arrhythmogenic right ventricular cardiomyopathy; Arrhythmogenic right ventricular cardiomyopathy
|CLNACC=RCV000000770.2; RCV000039375.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM; GeneReviews:MedGen:SNOMED_CT:SNOMED_CT
|CLNDSDBID=NBK1131:C1858379:604400; NBK1131:C0349788:253528005:281170005
}}

{{PMID|18313022|OA=1
}} Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}