{{Rsnum
|rsid=201936720
|Chromosome=17
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=POLG2
|position=64485733
|Gene_s=POLG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=17
|CLNACC=RCV000033246.2
|CLNALLE=1
|CLNDBN=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1864668:610131
|CLNHGVS=NC_000017.10:g.62481850T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604983.0004
|Disease=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4
|FwdALT=C
|FwdREF=T
|GENEINFO=POLG2:11232
|GENE_ID=11232
|GENE_NAME=POLG2
|REF=T
|RSPOS=62481850
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=201936720
}}