{{Rsnum
|rsid=121918052
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=POLG
|position=89327006
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MIR6766,POLG
}}{{omim
|id=174763
|rsnum=121918052
|variant=0016
}}{{ClinVar
|rsid=121918052
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=89870237
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=POLG:5428
|GENE_NAME=POLG
|GENE_ID=5428
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.89870237C>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000014464.23
|CLNDBN=Myoclonic epilepsy myopathy sensory ataxia
|CLNDSDB=MedGen
|CLNDSDBID=C1843852
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=174763.0016
|Disease=Myoclonic epilepsy myopathy sensory ataxia
}}