{{Rsnum
|rsid=387907139
|Chromosome=12
|position=94994249
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NDUFA12
|Gene_s=NDUFA12
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=12
|CLNACC=RCV000024206.1
|CLNALLE=1
|CLNDBN=Leigh syndrome due to mitochondrial complex I deficiency
|CLNDSDB=MedGen
|CLNDSDBID=C1838951
|CLNHGVS=NC_000012.11:g.95388025G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614530.0001
|Disease=Leigh syndrome due to mitochondrial complex I deficiency
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=95388025
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=387907139
|GENEINFO=NDUFA12:55967
|GENE_ID=55967
|GENE_NAME=NDUFA12
}}