CDH23 NM_022124.6(CDH23):c.9629_9632del (p.Ile3210fs)

CI-VAR-00008705Explore in graph →p.Ile3210fsNM_022124.6:c.9629_9632delClinVar 46077 rs397517367

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
46077	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Rare genetic deafness; Usher syndrome type 1; Pituitary adenoma 5, multiple types; CDH23-related disorder	germline	6	Jan 25, 2026	clinvar