{{Rsnum
|rsid=41460449
|Gene=ANKRD20A19P
|Chromosome=MT
|position=3394
|Orientation=plus
|GMAF=0.004677
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MT-ND1
}}{{ClinVar
|ALT=C
|CAF=0.9953; 0.004677
|CHROM=MT
|CLNACC=RCV000010375.2
|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.3394T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516000.0004
|COMMON=0
|Disease=Leber's optic atrophy
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=3394
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;HD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000402110100
|WGT=0
|dbSNPBuildID=127
|rsid=41460449
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}