{{Rsnum
|rsid=267606896
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=OR5AP2
|position=13084
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-CYB
}}{{ClinVar
|ALT=T
|CHROM=MT
|CLNACC=RCV000010343.1; RCV000010344.1
|CLNALLE=1
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency; Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
|CLNDSDB=MedGen; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1838951; NBK1224:NBK1233:C0162671:540000:550:39925003
|CLNHGVS=NC_012920.1:m.13084A>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516005.0006
|Disease=Leigh syndrome due to mitochondrial complex I deficiency; Juvenile myopathy
|FwdALT=T
|FwdREF=A
|REF=A
|RSPOS=13084
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606896
}}