SATB2 NM_001172509.2(SATB2):c.598-4del

CI-VAR-00109480Explore in graph →NM_001172509.2:c.598-4delClinVar 589489 rs199978702

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
589489	Likely benign	criteria provided, multiple submitters, no conflicts	2	Chromosome 2q32-q33 deletion syndrome; Inborn genetic diseases; Cholangiocarcinoma; Nonpapillary renal cell carcinoma	germline	3	Nov 26, 2025	clinvar