{{Rsnum
|rsid=121913038
|Chromosome=22
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TYMP
|position=50528571
|Gene_s=TYMP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=131222
|rsnum=121913038
|variant=0008
}}{{ClinVar
|rsid=121913038
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=50967000
|CHROM=22
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TYMP:1890
|GENE_NAME=TYMP
|GENE_ID=1890
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.50967000C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000018140.26
|CLNDBN=MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=131222.0008
|Disease=MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE)
}}