{{Rsnum
|rsid=113449357
|Gene=TMEM43
|Chromosome=3
|position=14139231
|Orientation=plus
|GMAF=0.006428
|Gene_s=TMEM43
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ClinVar
|rsid=113449357
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=14180731
|CHROM=3
|GMAF=0.0064
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000040416100100
|GENEINFO=TMEM43:79188
|GENE_NAME=TMEM43
|GENE_ID=79188
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.14180731C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Cardiomyopathy; AllHighlyPenetrant
|Disease=Cardiomyopathy; AllHighlyPenetrant
|Tags=PM;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD
|CAF=0.9936; 0.006428
|CLNACC=RCV000030555.1; RCV000039394.1
|CLNDSDB=MedGen:SNOMED_CT; MedGen
|CLNDSDBID=C0878544:85898001; CN169374
|COMMON=1
}}