Variant (rsID / SNP)

rs1057519625

rs1057519625 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53. Location: chromosome 17, position 7,573,976. Clinical significance in the table: drug response.

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Reference-table entries

TP53Drug response

Clinical significance (as recorded): drug response
Variant type: Deletion
Chromosome / position: 17:7573976
Cytoband: 17p13.1
HGVS: NM_000546.6(TP53):c.1044_1051del (p.Glu349fs)

Associated conditions / phenotypes

Poly (ADP-Ribose) polymerase inhibitor response

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.