{{Rsnum
|rsid=267606895
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=OR5AP2
|position=13045
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-CYB
}}{{ClinVar
|ALT=C
|CHROM=MT
|CLNACC=RCV000010340.1; RCV000010341.1; RCV000010342.2
|CLNALLE=1
|CLNDBN=Juvenile myopathy, encephalopathy, lactic acidosis AND stroke; Leber's optic atrophy; Leigh syndrome due to mitochondrial complex I deficiency
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1224:NBK1233:C0162671:540000:550:39925003; NBK1174:NBK1224:C0917796:535000:104:58610003; C1838951
|CLNHGVS=NC_012920.1:m.13045A>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516005.0005
|Disease=Juvenile myopathy; Leber's optic atrophy; Leigh syndrome due to mitochondrial complex I deficiency
|FwdALT=C
|FwdREF=A
|REF=A
|RSPOS=13045
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606895
}}