{{Rsnum
|rsid=104894630
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCO1
|position=10692805
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCO1
}}{{omim
|id=603644
|rsnum=104894630
|variant=0002
}}{{ClinVar
|rsid=104894630
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=10596122
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SCO1:6341
|GENE_NAME=SCO1
|GENE_ID=6341
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.10596122G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000006555.1
|CLNDBN=Hepatic failure, early-onset, and neurologic disorder due to cytochrome c oxidase deficiency
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603644.0002
|Disease=Hepatic failure
}}