{{Rsnum
|rsid=267606891
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SESN3
|position=10197
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-CO3
}}{{ClinVar
|ALT=A
|CHROM=MT
|CLNACC=RCV000010362.1; RCV000010363.3
|CLNALLE=1
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency; Leber hereditary optic neuropathy with dystonia
|CLNDSDB=MedGen; MedGen:OMIM:Orphanet
|CLNDSDBID=C1838951; C1839040:500001:99718
|CLNHGVS=NC_012920.1:m.10197G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516002.0004
|Disease=Leigh syndrome due to mitochondrial complex I deficiency; Leber hereditary optic neuropathy with dystonia
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=10197
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606891
}}