{{Rsnum
|rsid=199476122
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ANKRD20A19P
|position=3697
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-ND1
}}{{ClinVar
|ALT=A
|CHROM=MT
|CLNACC=RCV000010385.3; RCV000010386.1; RCV000056168.1
|CLNALLE=1
|CLNDBN=Juvenile myopathy, encephalopathy, lactic acidosis AND stroke; Leber hereditary optic neuropathy with dystonia; Leber's optic atrophy
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1224:NBK1233:C0162671:540000:550:39925003; C1839040:500001:99718; NBK1174:NBK1224:C0917796:535000:104:58610003
|CLNHGVS=NC_012920.1:m.3697G>A
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1174; 516000.0012
|Disease=Juvenile myopathy; Leber hereditary optic neuropathy with dystonia; Leber's optic atrophy
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=3697
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476122
}}