{{Rsnum
|rsid=111033572
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=C10orf2
|position=100989823
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=C10orf2
}}{{omim
|id=606075
|rsnum=111033572
|variant=0002
}}{{ClinVar
|rsid=111033572
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=102749580
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=C10orf2:56652
|GENE_NAME=C10orf2
|GENE_ID=56652
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.102749580G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606075.0002
|CLNSIG=5
|CLNCUI=C1836439
|CLNDBN=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
|Disease=Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
|CLNACC=RCV000004880.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1836439:609286
}}