Variant (rsID / SNP)

rs1060501287

rs1060501287 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BARD1. Location: chromosome 2, position 215,634,026. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

BARD1Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: Deletion
Chromosome / position: 2:215634026
Cytoband: 2q35
HGVS: NM_000465.4(BARD1):c.1325del (p.Pro442fs)

Associated conditions / phenotypes

Familial cancer of breast

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.