{{Rsnum
|rsid=121913041
|Chromosome=22
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=TYMP
|position=50527629
|Gene_s=SCO2,TYMP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=131222
|rsnum=121913041
|variant=0013
}}{{ClinVar
|rsid=121913041
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=50966058
|CHROM=22
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TYMP:1890; SCO2:9997
|GENE_NAME=TYMP; SCO2
|GENE_ID=1890; 9997
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.50966058C>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000018145.22
|CLNDBN=MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=131222.0013
|Disease=MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE)
}}