Variant (rsID / SNP)

rs202194596

rs202194596 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PALB2. Location: chromosome 16, position 23,649,272. Clinical significance in the table: Uncertain significance.

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Reference-table entries

PALB2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 16:23649272
Cytoband: 16p12.2
HGVS: NM_024675.4(PALB2):c.110G>A (p.Arg37His)
Allele change: Missense_R37H

Associated conditions / phenotypes

Familial cancer of breast|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.