{{Rsnum
|rsid=199476121
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ANKRD20A19P
|position=4136
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-CO1
}}{{ClinVar
|ALT=G
|CHROM=MT
|CLNACC=RCV000010378.1
|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.4136A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516000.0006
|Disease=Leber's optic atrophy
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=4136
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476121
}}