Variant (rsID / SNP)
rs56160474
rs56160474 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPYD. Location: chromosome 1, position 97,544,258. Clinical significance in the table: Benign.
Reference-table entries
DPYDBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:97544258
- Cytoband
- 1p21.3
- HGVS
- NM_000110.4(DPYD):c.*274T>C
- Allele change
- Silent
Associated conditions / phenotypes
Dihydropyrimidine dehydrogenase deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.