Variant (rsID / SNP)

rs876658381

rs876658381 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA1. Location: chromosome 17, position 41,251,894. Clinical significance in the table: Uncertain significance.

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Reference-table entries

BRCA1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 17:41251894
Cytoband: 17q21.31
HGVS: NM_007294.4(BRCA1):c.445G>A (p.Glu149Lys)
Allele change: Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Hereditary breast ovarian cancer 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.