{{Rsnum
|rsid=121918310
|Chromosome=8
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RRM2B
|position=102208210
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RRM2B
}}{{omim
|id=604712
|rsnum=121918310
|variant=0006
}}{{ClinVar
|rsid=121918310
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=103220438
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RRM2B:50484
|GENE_NAME=RRM2B
|GENE_ID=50484
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.103220438G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604712.0006
|CLNSIG=5
|CLNCUI=C2751319
|CLNDBN=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5
|Disease=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5
|CLNACC=RCV000005722.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2751319:613077
}}