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Variant (rsID / SNP)

rs45551636

PALB2

rs45551636 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PALB2. Location: chromosome 16, position 23,634,293. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PALB2Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
16:23634293
Cytoband
16p12.2
HGVS
NM_024675.4(PALB2):c.2993G>A (p.Gly998Glu)
Allele change
Missense_G998E

Associated conditions / phenotypes

Familial cancer of breast|Hereditary cancer-predisposing syndrome|Fanconi anemia complementation group N|Malignant tumor of breast|Hereditary breast ovarian cancer syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.