Variant (rsID / SNP)

rs147390019

rs147390019 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUDT15. Location: chromosome 13, position 48,619,856. 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: 13:48619856
Cytoband: 13q14.2
HGVS: NM_018283.4(NUDT15):c.416G>A (p.Arg139His)
Allele change: Silent

Associated conditions / phenotypes

Thiopurines, poor metabolism of, 2

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.