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Variant (rsID / SNP)

rs114968502

DPYD

rs114968502 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPYD. Location: chromosome 1, position 98,060,579. 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
1:98060579
Cytoband
1p21.3
HGVS
NM_000110.4(DPYD):c.958+36A>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.