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Variant (rsID / SNP)

rs28363284

RAD51D

rs28363284 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51D. Location: chromosome 17, position 33,430,313. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RAD51DBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
17:33430313
Cytoband
17q12
HGVS
NM_002878.4(RAD51D):c.698A>G (p.Glu233Gly)
Allele change
Silent

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Breast-ovarian cancer, familial, susceptibility to, 4|Malignant tumor of breast|Hereditary breast ovarian cancer syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.