{{Rsnum
|rsid=118192098
|Gene=FAM160B1
|Chromosome=MT
|position=8344
|Orientation=plus
|GMAF=0.0009355
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ClinVar
|ALT=G,T
|CAF=0.9991; 0.0009355
|CHROM=MT
|CLNACC=RCV000010192.5; RCV000010193.3; RCV000010194.3
|CLNALLE=1
|CLNDBN=Myoclonus with epilepsy with ragged red fibers; Leigh's disease; Parkinson disease, mitochondrial
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1224:NBK1520:C0162672:545000:551; NBK1173:NBK1203:NBK1224:C0023264:256000:ORPHA506:29570005; NBK1223:C1838867:556500
|CLNHGVS=NC_012920.1:m.8344A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=590060.0001
|COMMON=0
|Disease=Myoclonus with epilepsy with ragged red fibers; Leigh's disease; Parkinson disease
|FwdALT=G,T
|FwdREF=A
|REF=A
|RSPOS=8344
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=132
|rsid=118192098
}}