Variant (rsID / SNP)

rs876658983

rs876658983 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PALB2. Location: chromosome 16, position 23,637,612. Clinical significance in the table: Pathogenic.

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Reference-table entries

PALB2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 16:23637612
Cytoband: 16p12.2
HGVS: NM_024675.4(PALB2):c.2693G>A (p.Trp898Ter)
Allele change: Nonsense_W898X

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome

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.