Gene entry
RAD51D
RAD51 paralog D
- Chromosome
- 17
- Cytoband
- 17q12
- Variants (rsID)
- 27
RAD51D is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q12). Its official name is “RAD51 paralog D”. The reference table lists 27 variants (rsID) for this gene.
Clinically classified variants
23 reference-table entries with clinical significance.
- rs28363284Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4|Malignant tumor of breast|Hereditary breast ovarian cancer syndrome
- rs4796033Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4
- rs115031549Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Hereditary breast ovarian cancer syndrome|Breast-ovarian cancer, familial, susceptibility to, 4|Malignant tumor of breast
- rs138557828Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4
- rs138969595Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4
- rs140317560Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4|Hereditary breast ovarian cancer syndrome
- rs145309168Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4|Hereditary breast ovarian cancer syndrome|Malignant tumor of breast
- rs201141245Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4|Malignant tumor of breast
- rs374382703Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4
- rs45478491Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4|Hereditary breast ovarian cancer syndrome|Malignant tumor of breast
- rs56026142Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4|Hereditary breast ovarian cancer syndrome|Breast and/or ovarian cancer
- rs587782129Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4
- rs762247126Conflicting interpretationssingle nucleotide variantBreast-ovarian cancer, familial, susceptibility to, 4|Hereditary cancer-predisposing syndrome
- rs80116829Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4|Hereditary breast ovarian cancer syndrome|Malignant tumor of breast
- rs876659026Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome
- rs876659339Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4
- rs876659394Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4|Breast and/or ovarian cancer
- rs878854562Conflicting interpretationssingle nucleotide variantBreast-ovarian cancer, familial, susceptibility to, 4|Hereditary cancer-predisposing syndrome
- rs137886232Pathogenicsingle nucleotide variantBreast-ovarian cancer, familial, susceptibility to, 4|Hereditary cancer-predisposing syndrome|Breast carcinoma
- rs587782695Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4
- rs730881935PathogenicDeletionHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4|Hereditary breast ovarian cancer syndrome
- rs730882119PathogenicDuplicationBreast-ovarian cancer, familial, susceptibility to, 4|Hereditary cancer-predisposing syndrome
- rs786203137PathogenicDeletionHereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4
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.
