CDH23 NM_022124.6(CDH23):c.1143_1176del

CI-VAR-00205277Explore in graph →NM_022124.6:c.1143_1176delClinVar 1357019 rs764949139

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
1357019	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Usher syndrome type 1D; Autosomal recessive nonsyndromic hearing loss 12; Pituitary adenoma 5, multiple types	germline	3	Jan 21, 2023	clinvar