Variant (rsID / SNP)

rs397509132

rs397509132 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA1. Location: chromosome 17, position 41,243,496. Clinical significance in the table: Pathogenic.

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Reference-table entries

BRCA1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 17:41243496
Cytoband: 17q21.31
HGVS: NM_007294.4(BRCA1):c.4052T>A (p.Leu1351Ter)
Allele change: Silent

Associated conditions / phenotypes

Breast-ovarian cancer, familial, susceptibility to, 1|Breast and/or ovarian cancer

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.