{{Rsnum
|rsid=113994161
|Chromosome=13
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SUCLA2
|position=47988540
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SUCLA2
}}{{omim
|id=603921
|rsnum=113994161
|variant=0002
}}{{ClinVar
|rsid=113994161
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=48562675
|CHROM=13
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050160000000000002110100
|GENEINFO=SUCLA2:8803
|GENE_NAME=SUCLA2
|GENE_ID=8803
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.48562675C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK6803; 603921.0002
|CLNSIG=5
|CLNCUI=C2677554
|CLNDBN=Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)
|Disease=Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)
|CLNACC=RCV000020560.2
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK6803:C2749864:612073:1933
}}