Variant (rsID / SNP)

rs769414858

rs769414858 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PALB2. Location: chromosome 16, position 23,634,281. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PALB2Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: Deletion
Chromosome / position: 16:23634281
Cytoband: 16p12.2
HGVS: NM_024675.4(PALB2):c.2996+9del

Associated conditions / phenotypes

Familial cancer of breast|Hereditary cancer-predisposing syndrome|Malignant tumor of breast

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.