Variant (rsID / SNP)
rs1064793929
rs1064793929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53. Location: chromosome 17, position 7,578,485. Clinical significance in the table: Pathogenic.
Reference-table entries
TP53Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 17:7578485
- Cytoband
- 17p13.1
- HGVS
- NM_000546.6(TP53):c.445del (p.Ser149fs)
Associated conditions / phenotypes
Neoplasm of ovary
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.