{{Rsnum
|rsid=386834147
|Chromosome=10
|position=100988457
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=C10orf2
|Gene_s=C10orf2,MRPL43
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=T
|CHROM=10
|CLNACC=RCV000050141.1
|CLNALLE=1
|CLNDBN=Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK3795:C1849096:271245:1186
|CLNHGVS=NC_000010.10:g.102748214C>T
|CLNSIG=4
|Disease=Mitochondrial DNA depletion syndrome 7 (hepatocerebral type)
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=102748214
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386834147
|GENEINFO=MRPL43:84545; C10orf2:56652
|GENE_ID=84545; 56652
|GENE_NAME=MRPL43; C10orf2
}}{{PMID Auto
|PMID=22928142
|Title=Novel Autosomal Recessive c10orf2 Mutations Causing Infantile-Onset Spinocerebellar Ataxia.
|OA=1
}}