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Gene entry

BARD1

BRCA1 associated RING domain 1

Chromosome
2
Cytoband
2q35
Variants (rsID)
50

BARD1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q35). Its official name is “BRCA1 associated RING domain 1”. The reference table lists 50 variants (rsID) for this gene.

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Clinically classified variants

32 reference-table entries with clinical significance.

  • rs370359540Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast|Malignant tumor of breast
  • rs144856889Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast|Malignant tumor of breast
  • rs146946984Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast|Malignant tumor of breast
  • rs370000575Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs370771157Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs3738888Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast|Triple-Negative Breast Cancer Finding|Malignant tumor of breast|Hereditary breast ovarian cancer syndrome
  • rs570022823Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs587780035Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs587781976Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast|Hereditary breast ovarian cancer syndrome
  • rs587782555Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs730881413Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast|Hereditary breast ovarian cancer syndrome
  • rs752514155Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs753479021Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast|Familial pancreatic carcinoma
  • rs76744638Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast|Malignant tumor of breast|Hereditary breast ovarian cancer syndrome
  • rs780627045Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs886055601Conflicting interpretationssingle nucleotide variantFamilial cancer of breast|Hereditary cancer-predisposing syndrome
  • rs145063973Likely benignsingle nucleotide variantHereditary cancer-predisposing syndrome
  • rs75146556Likely benignsingle nucleotide variant
  • rs863224673Likely benignsingle nucleotide variantFamilial cancer of breast|Hereditary cancer-predisposing syndrome
  • rs864622239Likely pathogenicsingle nucleotide variantFamilial cancer of breast
  • rs1057517589PathogenicMicrosatelliteFamilial cancer of breast|Hereditary cancer-predisposing syndrome|Malignant tumor of breast
  • rs1060501287PathogenicDeletionFamilial cancer of breast
  • rs587780033PathogenicDuplicationHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs587781430Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs587782504PathogenicDeletionHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs587782897PathogenicDeletionHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs779427628PathogenicMicrosatelliteHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs786201912Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs786202500Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Familial cancer of breast
  • rs864622223PathogenicDeletionFamilial cancer of breast|Hereditary cancer-predisposing syndrome|Malignant tumor of breast
  • rs876659572PathogenicDeletionHereditary cancer-predisposing syndrome|Familial cancer of breast|Malignant tumor of breast
  • rs876660061PathogenicDeletionHereditary cancer-predisposing syndrome|Familial cancer of breast

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.