{{Rsnum
|rsid=121918136
|Chromosome=3
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NDUFAF3
|position=49022146
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DALRD3,NDUFAF3
}}{{omim
|id=612911
|rsnum=121918136
|variant=0003
}}{{ClinVar
|rsid=121918136
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=49059579
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MIR425:494337; DALRD3:55152; NDUFAF3:25915; MIR191:406966
|GENE_NAME=MIR425; DALRD3; NDUFAF3; MIR191
|GENE_ID=494337; 55152; 25915; 406966
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.49059579T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612911.0003
|CLNSIG=5
|CLNCUI=C1838979
|CLNDBN=Mitochondrial complex I deficiency
|Disease=Mitochondrial complex I deficiency
|CLNACC=RCV000000452.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1838979:252010
}}