{{Rsnum
|rsid=118192104
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FAM160B1
|position=8361
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=A
|CHROM=MT
|CLNACC=RCV000010202.2
|CLNALLE=1
|CLNDBN=Myoclonus with epilepsy with ragged red fibers
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1224:NBK1520:C0162672:545000:551
|CLNHGVS=NC_012920.1:m.8361G>A
|CLNSIG=5
|CLNSRC=GTR; OMIM Allelic Variant
|CLNSRCID=GTR000500598; 590060.0007
|Disease=Myoclonus with epilepsy with ragged red fibers
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=8361
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=132
|rsid=118192104
}}