{{Rsnum
|rsid=121434479
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NDUFS7
|position=1391144
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NDUFS7
}}{{omim
|id=601825
|rsnum=121434479
|variant=0002
}}{{ClinVar
|rsid=121434479
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=1391143
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NDUFS7:374291
|GENE_NAME=NDUFS7
|GENE_ID=374291
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.1391143G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601825.0002
|CLNSIG=5
|CLNCUI=C1838951
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency
|Disease=Leigh syndrome due to mitochondrial complex I deficiency
|CLNACC=RCV000008121.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1838951
}}