{{Rsnum
|rsid=121913039
|Gene=TYMP
|Chromosome=22
|position=50527612
|Orientation=minus
|GMAF=0.0004591
|Gene_s=SCO2,TYMP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{omim
|id=131222
|rsnum=121913039
|variant=0011
}}{{ClinVar
|rsid=121913039
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=50966041
|CHROM=22
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=TYMP:1890; SCO2:9997
|GENE_NAME=TYMP; SCO2
|GENE_ID=1890; 9997
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.50966041C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNACC=RCV000018143.22
|CLNDBN=MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=131222.0011
|COMMON=0
|Disease=MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE)
}}