{{Rsnum
|rsid=267606894
|Gene=OR5AP2
|Chromosome=MT
|position=12770
|Orientation=plus
|GMAF=0.0009346
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MT-CYB
}}{{ClinVar
|ALT=G
|CAF=0.9991; 0.0009346
|CHROM=MT
|CLNACC=RCV000010339.1
|CLNALLE=1
|CLNDBN=Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1224:NBK1233:C0162671:540000:550:39925003
|CLNHGVS=NC_012920.1:m.12770A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516005.0004
|COMMON=0
|Disease=Juvenile myopathy
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=12770
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606894
}}