{{Rsnum
|rsid=113994097
|Chromosome=15
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=POLG
|position=89323426
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=POLG
}}{{omim
|id=174763
|rsnum=113994097
|variant=0013
}}{{ClinVar
|rsid=113994097
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=89866657
|CHROM=15
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=POLG:5428
|GENE_NAME=POLG
|GENE_ID=5428
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.89866657C>G
|CLNSRC=Emory University; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=11673; NBK26471; 174763.0013
|CLNSIG=5
|CLNCUI=C1843851; C1843851
|CLNDBN=Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis; Myoclonic epilepsy myopathy sensory ataxia; Progressive sclerosing poliodystrophy; not provided
|Disease=Sensory ataxic neuropathy; Myoclonic epilepsy myopathy sensory ataxia; Progressive sclerosing poliodystrophy; not provided
|CLNACC=RCV000014459.24; RCV000014460.23; RCV000014461.16; RCV000080023.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK26471:NBK3795:C1843851:607459:ORPHA254818; C1843852; NBK26471:C0205710:203700:726:20415001
}}