{{Rsnum
|rsid=267606897
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OR5AP2
|position=13513
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-CYB
}}{{ClinVar
|ALT=A
|CHROM=MT
|CLNACC=RCV000010345.3; RCV000010346.2
|CLNALLE=1
|CLNDBN=Juvenile myopathy, encephalopathy, lactic acidosis AND stroke; Leigh syndrome due to mitochondrial complex I deficiency
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1224:NBK1233:C0162671:540000:550:39925003; C1838951
|CLNHGVS=NC_012920.1:m.13513G>A
|CLNSIG=5
|CLNSRC=GTR; OMIM Allelic Variant
|CLNSRCID=GTR000500597; 516005.0007
|Disease=Juvenile myopathy; Leigh syndrome due to mitochondrial complex I deficiency
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=13513
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606897
}}