Variant (rsID / SNP)
rs373321719
rs373321719 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PALB2. Location: chromosome 16, position 23,640,515. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
PALB2Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 16:23640515
- Cytoband
- 16p12.2
- HGVS
- NM_024675.4(PALB2):c.2586+10A>G
- Allele change
- Silent
Associated conditions / phenotypes
Familial cancer of breast|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group N|Endometrial carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.