{{Rsnum
|rsid=118192101
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FAM160B1
|position=8313
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=A
|CHROM=MT
|CLNACC=RCV000010200.3
|CLNALLE=1
|CLNDBN=Mitochondrial neurogastrointestinal encephalomyopathy syndrome
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1179:NBK26471:C0872218:603041:298
|CLNHGVS=NC_012920.1:m.8313G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=590060.0004
|Disease=Mitochondrial neurogastrointestinal encephalomyopathy syndrome
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=8313
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=132
|rsid=118192101
}}