{{Rsnum
|rsid=104893898
|Chromosome=5
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NDUFS4
|position=53646371
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NDUFS4
}}{{omim
|id=602694
|rsnum=104893898
|variant=0003
}}{{ClinVar
|rsid=104893898
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=52942201
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NDUFS4:4724
|GENE_NAME=NDUFS4
|GENE_ID=4724
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.52942201C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602694.0003
|CLNSIG=5
|CLNCUI=C1838951
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency
|Disease=Leigh syndrome due to mitochondrial complex I deficiency
|CLNACC=RCV000007292.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1838951
}}