{{Rsnum
|rsid=199476109
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CCDC152
|position=14487
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-CYB
}}{{ClinVar
|ALT=C
|CHROM=MT
|CLNACC=RCV000010333.1; RCV000010334.1
|CLNALLE=1
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency; Striatal necrosis, bilateral, with dystonia
|CLNDSDB=MedGen
|CLNDSDBID=C1838951
|CLNHGVS=NC_012920.1:m.14487T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516006.0007
|Disease=Leigh syndrome due to mitochondrial complex I deficiency; Striatal necrosis
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=14487
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476109
}}