{{Rsnum
|rsid=199592341
|Gene=NDUFA9
|Chromosome=12
|position=4685324
|Orientation=plus
|GMAF=0.0004591
|Gene_s=NDUFA9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=A,C
|CAF=0.9995; 0.0004591; .
|CHROM=12
|CLNACC=RCV000023344.1
|CLNALLE=2
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency
|CLNDSDB=MedGen
|CLNDSDBID=C1838951
|CLNHGVS=NC_000012.11:g.4794490G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603834.0001
|COMMON=0
|Disease=Leigh syndrome due to mitochondrial complex I deficiency
|FwdALT=A,C
|FwdREF=G
|GENEINFO=NDUFA9:4704
|GENE_ID=4704
|GENE_NAME=NDUFA9
|REF=G
|RSPOS=4794490
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000016100100
|WGT=0
|dbSNPBuildID=137
|rsid=199592341
}}