{{Rsnum
|rsid=121909300
|Chromosome=5
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=OXCT1
|position=41749579
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OXCT1
}}{{omim
|id=601424
|rsnum=121909300
|variant=0002
}}{{ClinVar
|rsid=121909300
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=41749681
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=OXCT1:5019
|GENE_NAME=OXCT1
|GENE_ID=5019
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.41749681C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601424.0002
|CLNSIG=5
|CLNCUI=C0342792
|CLNDBN=Succinyl-CoA acetoacetate transferase deficiency
|Disease=Succinyl-CoA acetoacetate transferase deficiency
|CLNACC=RCV000008642.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0342792:245050:832:238004006
}}