{{Rsnum
|rsid=104894884
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NDUFA1
|position=119871933
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NDUFA1,RNF113A
}}{{omim
|id=300078
|rsnum=104894884
|variant=0001
}}{{ClinVar
|rsid=104894884
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=119005896
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RNF113A:7737; NDUFA1:4694
|GENE_NAME=RNF113A; NDUFA1
|GENE_ID=7737; 4694
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.119005896G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300078.0001
|CLNSIG=5
|CLNCUI=C1838979
|CLNDBN=Mitochondrial complex I deficiency
|Disease=Mitochondrial complex I deficiency
|CLNACC=RCV000012414.15
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1838979:252010
}}