{{Rsnum
|rsid=387906426
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PFDN5
|position=4640
|Gene_s=PFDN5
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=A
|CHROM=MT
|CLNACC=RCV000010366.2
|CLNALLE=1
|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.4640C>A
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1174; 516001.0003
|Disease=Leber's optic atrophy
|FwdALT=A
|FwdREF=C
|REF=C
|RSPOS=4640
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906426
}}