CDH23 NC_000010.11:g.71682535dup

CI-VAR-00037376Explore in graph →ClinVar 228328 rs753886326

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
228328	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Rare genetic deafness; Usher syndrome; Usher syndrome type 1D; Pituitary adenoma 5, multiple types; Autosomal recessive nonsyndromic hearing loss 12	germline	3	Mar 13, 2024	clinvar