Variant (rsID / SNP)
rs145548112
rs145548112 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPYD, DPYD-AS1. Location: chromosome 1, position 97,771,751. The table records no clinical significance for this variant.
Reference-table entries
DPYDNot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:97771751
- Cytoband
- 1p21.3
- HGVS
- NM_000110.4(DPYD):c.2161G>A (p.Ala721Thr)
- Allele change
- Missense_A721T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.