{{Rsnum
|rsid=104894632
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=POLG2
|position=64477929
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MILR1,POLG2
}}{{omim
|id=604983
|rsnum=104894632
|variant=0001
}}{{ClinVar
|rsid=104894632
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=62474046
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=POLG2:11232
|GENE_NAME=POLG2
|GENE_ID=11232
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.62474046C>T
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604983.0001
|CLNSIG=5
|CLNCUI=C1864668; C1864668
|CLNDBN=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4
|Disease=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4
|CLNACC=RCV000005594.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1864668:610131
|CLNORIGIN=1
}}