Variant (rsID / SNP)

rs273902770

rs273902770 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRCA1. Location: chromosome 17, position 41,197,828. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

BRCA1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: Microsatellite
Chromosome / position: 17:41197828
Cytoband: 17q21.31
HGVS: NM_007294.4(BRCA1):c.5468-10_5468-9del

Associated conditions / phenotypes

Breast-ovarian cancer, familial, susceptibility to, 1|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.