Variant (rsID / SNP)
rs72728438
rs72728438 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPYD. Location: chromosome 1, position 97,847,874. Clinical significance in the table: Benign.
Reference-table entries
DPYDBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:97847874
- Cytoband
- 1p21.3
- HGVS
- NM_000110.4(DPYD):c.1974+75A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.