{{Rsnum
|rsid=111033577
|Chromosome=10
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=C10orf2
|position=100989352
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=C10orf2,MRPL43
}}{{omim
|id=606075
|rsnum=111033577
|variant=0007
}}{{ClinVar
|rsid=111033577
|Reversed=0
|FwdREF=T
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=102749109
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MRPL43:84545; C10orf2:56652
|GENE_NAME=MRPL43; C10orf2
|GENE_ID=84545; 56652
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.102749109T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606075.0007
|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=RCV000004885.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1836439:609286
}}