{{Rsnum
|rsid = 28931613
|Gene=TYMP
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=22
|position=50529579
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TYMP
}}{{omim
|desc=MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOMYOPATHY SYNDROME
|id=131222
|rsnum=28931613
|variant=0009
}}

{{ClinVar
|rsid=28931613
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=50968008
|CHROM=22
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050260000000000502110100
|GENEINFO=TYMP:1890
|GENE_NAME=TYMP
|GENE_ID=1890
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.50968008C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;HD;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000018141.26
|CLNDBN=MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=131222.0009
|Disease=MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE)
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}