{{Rsnum
|rsid=199476108
|Gene=CCDC152
|Chromosome=MT
|position=14482
|Orientation=plus
|GMAF=0.002806
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=MT-CYB
}}{{ClinVar
|ALT=A,G,T
|CAF=0.9972; 0.002806
|CHROM=MT
|CLNACC=RCV000010332.2; RCV000055701.1
|CLNALLE=1; 2
|CLNDBN=Leber's optic atrophy
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1174:NBK1224:C0917796:535000:104:58610003
|CLNHGVS=NC_012920.1:m.14482C>A; NC_012920.1:m.14482C>G
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1174; 516006.0006
|COMMON=0
|Disease=Leber's optic atrophy
|FwdALT=A,G,T
|FwdREF=C
|REF=C
|RSPOS=14482
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476108
}}