Variant (rsID / SNP)

rs2669429

rs2669429 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPYS. Location: chromosome 8, position 105,463,690. The table records no clinical significance for this variant.

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Reference-table entries

DPYSNot classified

Variant type: single nucleotide variant
Chromosome / position: 8:105463690
Cytoband: 8q22.3
HGVS: NM_001385.3(DPYS):c.265-58T>C
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.