{{Rsnum
|rsid=74315511
|Chromosome=22
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SCO2
|position=50523994
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NCAPH2,SCO2
}}{{omim
|id=604272
|rsnum=74315511
|variant=0002
}}{{ClinVar
|rsid=74315511
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=50962423
|CHROM=22
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SCO2:9997; NCAPH2:29781
|GENE_NAME=SCO2; NCAPH2
|GENE_ID=9997; 29781
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.50962423C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604272.0002
|CLNSIG=5
|CLNCUI=C1858424
|CLNDBN=Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency; Myopia 6
|Disease=Cardioencephalomyopathy; Myopia 6
|CLNACC=RCV000006035.2; RCV000043619.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen:OMIM
|CLNDSDBID=C1858424:604377:1561; C1837148:608908
}}