{{Rsnum
|rsid=118203884
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HTR3C
|position=4409
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=C
|CHROM=MT
|CLNACC=RCV000010191.1
|CLNALLE=1
|CLNDBN=Mitochondrial myopathy
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1224:C0162670:251900
|CLNHGVS=NC_012920.1:m.4409T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=590065.0001
|Disease=Mitochondrial myopathy
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=4409
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=132
|rsid=118203884
}}