{{Rsnum
|rsid=121912638
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NDUFS8
|position=68033216
|Gene_s=NDUFS8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121912638
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=67800683
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MIR4691:100616403; NDUFS8:4728
|GENE_NAME=MIR4691; NDUFS8
|GENE_ID=100616403; 4728
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.67800683G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602141.0002
|CLNSIG=5
|CLNCUI=C1838951
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency
|Disease=Leigh syndrome due to mitochondrial complex I deficiency
|CLNACC=RCV000007942.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1838951
}}