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Variant (rsID / SNP)

rs149522412

PALB2

rs149522412 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PALB2. Location: chromosome 16, position 23,634,435. 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
single nucleotide variant
Chromosome / position
16:23634435
Cytoband
16p12.2
HGVS
NM_024675.4(PALB2):c.2851T>C (p.Ser951Pro)
Allele change
Missense_S951P

Associated conditions / phenotypes

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

Public references

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