{{Rsnum
|rsid=199476105
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CCDC152
|position=14459
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-CYB
}}{{ClinVar
|ALT=A
|CHROM=MT
|CLNACC=RCV000010326.1; RCV000010327.2; RCV000010328.3
|CLNALLE=1
|CLNDBN=Leber hereditary optic neuropathy with dystonia; Leber's optic atrophy; Leigh syndrome due to mitochondrial complex I deficiency
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=C1839040:500001:99718; NBK1174:NBK1224:C0917796:535000:104:58610003; C1838951
|CLNHGVS=NC_012920.1:m.14459G>A
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1174; 516006.0002
|Disease=Leber hereditary optic neuropathy with dystonia; Leber's optic atrophy; Leigh syndrome due to mitochondrial complex I deficiency
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=14459
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476105
}}