{{Rsnum
|rsid=121434428
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=NDUFS2
|position=161209915
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NDUFS2
}}{{omim
|id=602985
|rsnum=121434428
|variant=0002
}}{{ClinVar
|rsid=121434428
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=161209915
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=NDUFS2:4720
|GENE_NAME=NDUFS2
|GENE_ID=4720
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.161209915C>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_004550.4:c.686C>A; 602985.0002
|CLNSIG=5
|CLNCUI=C1838979
|CLNDBN=Mitochondrial complex I deficiency
|Disease=Mitochondrial complex I deficiency
|CLNACC=RCV000007102.1
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1838979:252010
}}