Variant (rsID / SNP)

rs115632870

rs115632870 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPYD. Location: chromosome 1, position 98,293,821. The table records no clinical significance for this variant.

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Reference-table entries

DPYDNot classified

Variant type: single nucleotide variant
Chromosome / position: 1:98293821
Cytoband: 1p21.3
HGVS: NM_000110.4(DPYD):c.151-69G>A
Allele change: Silent

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.