{{Rsnum
|rsid=397514618
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NDUFS8
|position=68033000
|Gene_s=MIR4691,NDUFS8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000033056.2
|CLNALLE=1
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency
|CLNDSDB=MedGen
|CLNDSDBID=C1838951
|CLNHGVS=NC_000011.9:g.67800467G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602141.0007
|Disease=Leigh syndrome due to mitochondrial complex I deficiency
|FwdALT=C
|FwdREF=G
|GENEINFO=MIR4691:100616403; NDUFS8:4728
|GENE_ID=100616403; 4728
|GENE_NAME=MIR4691; NDUFS8
|REF=G
|RSPOS=67800467
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=397514618
}}