{{Rsnum
|rsid=387906422
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=C14orf182
|position=8528
|Gene_s=C14orf182
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=C
|CHROM=MT
|CLNACC=RCV000010272.2
|CLNALLE=1
|CLNDBN=Cardiomyopathy, infantile hypertrophic
|CLNHGVS=NC_012920.1:m.8528T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516060.0010; 516070.0003
|Disease=Cardiomyopathy
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=8528
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=387906422
}}