{{Rsnum
|rsid=121908537
|Chromosome=13
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SUCLA2
|position=47988901
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SUCLA2
}}{{omim
|id=603921
|rsnum=121908537
|variant=0003
}}{{ClinVar
|rsid=121908537
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=48563036
|CHROM=13
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SUCLA2:8803
|GENE_NAME=SUCLA2
|GENE_ID=8803
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.48563036C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000006343.1
|CLNDBN=Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603921.0003
|Disease=Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK6803:C2749864:612073:1933
}}