{{Rsnum
|rsid=28616230
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=ANKRD20A19P
|position=4171
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-CO1
}}{{ClinVar
|ALT=A,T
|CHROM=MT
|CLNACC=RCV000010384.4
|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.4171C>A
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1174; 516000.0010
|Disease=Leber's optic atrophy
|FwdALT=A,T
|FwdREF=C
|REF=C
|RSPOS=4171
|Reversed=0
|SAO=0
|SSR=1
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=125
|rsid=28616230
}}