Variant (rsID / SNP)

rs886039675

rs886039675 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA1. Location: chromosome 17, position 41,197,718. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

BRCA1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: Deletion
Chromosome / position: 17:41197718
Cytoband: 17q21.31
HGVS: NM_007294.4(BRCA1):c.5569del (p.Gln1857fs)

Associated conditions / phenotypes

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.