BRWD3 NM_153252.5(BRWD3):c.2325+5G>A

CI-VAR-00046406Explore in graph →NM_153252.5:c.2325+5G>AClinVar 252790 rs186391561

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
252790	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Intellectual disability, X-linked 93; Inborn genetic diseases; Familial pancreatic carcinoma; Colon adenocarcinoma; Gastric cancer; Lymphoma; Cervical cancer; Clear cell carcinoma of kidney; Acute myeloid leukemia; Familial cancer of breast	germline	11	Feb 03, 2026	clinvar