{{Rsnum
|rsid=199474672
|Chromosome=MT
|Orientation=plus
|geno1=(AG;AG)
|geno2=(AG;T)
|geno3=(T;T)
|Gene=SMR3B
|position=5537
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=AT
|CHROM=MT
|CLNACC=RCV000010164.1; RCV000010165.1
|CLNALLE=1
|CLNDBN=Encephalopathy, mitochondrial; Leigh's disease
|CLNDSDB=MedGen; GeneReviews:GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1852373; NBK1173:NBK1203:NBK1224:C0023264:256000:ORPHA506:29570005
|CLNHGVS=NC_012920.1:m.5537_5538insT
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=590095.0002
|Disease=Encephalopathy; Leigh's disease
|FwdALT=T
|FwdREF=A
|REF=A
|RSPOS=5537
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=138
|rsid=199474672
}}