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Variant (rsID / SNP)

rs45511291

RAD51C

rs45511291 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAD51C. Location: chromosome 17, position 56,772,341. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RAD51CBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
17:56772341
Cytoband
17q22
HGVS
NM_058216.3(RAD51C):c.195A>G (p.Arg65=)
Allele change
Silent

Associated conditions / phenotypes

Fanconi anemia complementation group O|Hereditary cancer-predisposing syndrome|Fanconi anemia|Breast and Ovarian Cancer Susceptibility|Breast-ovarian cancer, familial, susceptibility to, 3|Malignant tumor of breast

Public references

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