{{Rsnum
|rsid=121434429
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NDUFS2
|position=161213673
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FCER1G,NDUFS2
}}{{omim
|id=602985
|rsnum=121434429
|variant=0003
}}{{ClinVar
|rsid=121434429
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=161213673
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260020a05000002110100
|GENEINFO=NDUFS2:4720; FCER1G:2207
|GENE_NAME=NDUFS2; FCER1G
|GENE_ID=4720; 2207
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.161213673T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_004106.1:c.-1649T>C; NM_004550.4:c.1237T>C; 602985.0003
|CLNSIG=5
|CLNCUI=C1838979
|CLNDBN=Mitochondrial complex I deficiency
|Disease=Mitochondrial complex I deficiency
|CLNACC=RCV000007103.1
|Tags=PM;S3D;NSM;REF;R5;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1838979:252010
}}