Variant (rsID / SNP)

rs25487

rs25487 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XRCC1. Location: chromosome 19, position 44,055,726. Clinical significance in the table: drug response.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

XRCC1Drug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 19:44055726
Cytoband: 19q13.31
HGVS: NM_006297.3(XRCC1):c.1196A>G (p.Gln399Arg)
Allele change: Missense_Q399R

Associated conditions / phenotypes

Platinum compounds response - Efficacy|Spinocerebellar ataxia, autosomal recessive 26

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.