{{Rsnum
|rsid=118192099
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FAM160B1
|position=8356
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=C
|CHROM=MT
|CLNACC=RCV000010195.3; RCV000010196.3
|CLNALLE=1
|CLNDBN=Myoclonus with epilepsy with ragged red fibers; MERRF/MELAS overlap syndrome
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1224:NBK1520:C0162672:545000:551; CN069283
|CLNHGVS=NC_012920.1:m.8356T>C
|CLNSIG=5
|CLNSRC=GTR; OMIM Allelic Variant
|CLNSRCID=GTR000500598; 590060.0002
|Disease=Myoclonus with epilepsy with ragged red fibers; MERRF/MELAS overlap syndrome
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=8356
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=132
|rsid=118192099
}}