{{Rsnum
|rsid = 28939714
|Gene = NDUFS3
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=11
|position=47582140
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NDUFS3
}}{{omim
|desc=LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
|id=603846
|rsnum=28939714
|variant=0001
}}{{ClinVar
|rsid=28939714
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=47603692
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NDUFS3:4722
|GENE_NAME=NDUFS3
|GENE_ID=4722
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.47603692C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603846.0001
|CLNSIG=5
|CLNCUI=C1838951
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency
|Disease=Leigh syndrome due to mitochondrial complex I deficiency
|CLNACC=RCV000006390.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1838951
}}