{{Rsnum
|rsid=118203929
|Chromosome=20
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=C20orf7
|position=13801652
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NDUFAF5
}}{{omim
|id=612360
|rsnum=118203929
|variant=0001
}}{{ClinVar
|rsid=118203929
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=13782298
|CHROM=20
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NDUFAF5:79133
|GENE_NAME=NDUFAF5
|GENE_ID=79133
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.13782298T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612360.0001
|CLNSIG=5
|CLNCUI=C1838979
|CLNDBN=Mitochondrial complex I deficiency
|Disease=Mitochondrial complex I deficiency
|CLNACC=RCV000000600.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1838979:252010
}}