Variant (rsID / SNP)

rs116855232

rs116855232 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUDT15. Location: chromosome 13, position 48,619,855. Clinical significance in the table: drug response.

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Reference-table entries

NUDT15Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 13:48619855
Cytoband: 13q14.2
HGVS: NM_018283.4(NUDT15):c.415C>T (p.Arg139Cys)
Allele change: Silent

Associated conditions / phenotypes

Thiopurines, poor metabolism of, 2|azathioprine response - Toxicity|mercaptopurine response - Dosage

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.