{{Rsnum
|rsid=267606893
|Chromosome=MT
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=OR5AP2
|position=12706
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-ND5
}}{{ClinVar
|ALT=C
|CHROM=MT
|CLNACC=RCV000010338.1
|CLNALLE=1
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency
|CLNDSDB=MedGen
|CLNDSDBID=C1838951
|CLNHGVS=NC_012920.1:m.12706T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516005.0003
|Disease=Leigh syndrome due to mitochondrial complex I deficiency
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=12706
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;HD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000402110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606893
}}