Variant (rsID / SNP)

rs886040168

rs886040168 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA1. Location: chromosome 17, position 41,243,708. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

BRCA1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 17:41243708
Cytoband: 17q21.31
HGVS: NM_007294.4(BRCA1):c.3837_3840del (p.Ser1280fs)

Associated conditions / phenotypes

Breast-ovarian cancer, familial, susceptibility to, 1

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.