RAD51C NM_058216.3(RAD51C):c.905-2_905-1del

CI-VAR-00023586Explore in graph →NM_058216.3:c.905-2_905-1delClinVar 141768 rs587781995

Curated evidence

Evidence by cancer (0 items)

Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.

Data not yet available

No curated evidence item references this variant yet.

ClinVar

Clinical significance (1)

ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
141768	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Fanconi anemia complementation group O; Breast-ovarian cancer, familial, susceptibility to, 3; Breast and/or ovarian cancer; Hereditary breast ovarian cancer syndrome	germline	23	Feb 25, 2026	clinvar