{{Rsnum
|rsid = 28939711
|Gene = COX15
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=10
|position=99724057
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=COX15
}}{{omim
|desc=CARDIOMYOPATHY, HYPERTROPHIC, EARLY-ONSET FATAL
|id=603646
|rsnum=28939711
|variant=0001
}}{{ClinVar
|rsid=28939711
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=101483814
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=COX15:1355
|GENE_NAME=COX15
|GENE_ID=1355
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.101483814G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603646.0001
|CLNSIG=5
|CLNCUI=C1850599
|CLNDBN=Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2; Congenital myasthenic syndrome, acetazolamide-responsive
|Disease=Cardioencephalomyopathy; Congenital myasthenic syndrome
|CLNACC=RCV000006551.1; RCV000033252.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN166800:615119:1561; C1850599:614198:590
}}