{{Rsnum
|rsid=387906424
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=ZSCAN12
|position=14596
|Gene_s=ZSCAN12
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=T
|CHROM=MT
|CLNACC=RCV000010329.1; RCV000055704.1
|CLNALLE=1
|CLNDBN=Leber hereditary optic neuropathy with dystonia; Leber's optic atrophy
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1839040:500001:99718; NBK1174:NBK1224:C0917796:535000:104:58610003
|CLNHGVS=NC_012920.1:m.14596A>T
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1174; 516006.0003
|Disease=Leber hereditary optic neuropathy with dystonia; Leber's optic atrophy
|FwdALT=T
|FwdREF=A
|REF=A
|RSPOS=14596
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906424
}}