{{Rsnum
|rsid=121918051
|Chromosome=15
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=POLG
|position=89320878
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=POLG
}}{{omim
|id=174763
|rsnum=121918051
|variant=0014
}}{{ClinVar
|rsid=121918051
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=89864109
|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.89864109C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=174763.0014
|CLNSIG=5
|CLNCUI=C1834846
|CLNDBN=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1
|Disease=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1
|CLNACC=RCV000014462.16
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK1203:NBK26471:C1834846:157640
}}