Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs183489969

PALB2

rs183489969 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PALB2. Location: chromosome 16, position 23,632,742. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

PALB2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:23632742
Cytoband
16p12.2
HGVS
NM_024675.4(PALB2):c.3054G>C (p.Glu1018Asp)
Allele change
Missense_E1018D

Associated conditions / phenotypes

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

Public references

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