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Variant (rsID / SNP)

rs876658362

BRCA1

rs876658362 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA1. Location: chromosome 17, position 41,267,745. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

BRCA1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
17:41267745
Cytoband
17q21.31
HGVS
NM_007294.4(BRCA1):c.132C>T (p.Cys44_Lys45=)
Allele change
Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 1|Hereditary breast ovarian cancer syndrome

Public references

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