CDH23 NM_022124.6(CDH23):c.6050-9G>A

CI-VAR-00008694Explore in graph →NM_022124.6:c.6050-9G>AClinVar 46001 rs367928692

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
46001	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Rare genetic deafness; Usher syndrome type 1D; Pituitary adenoma 5, multiple types; Autosomal recessive nonsyndromic hearing loss 12; Usher syndrome type 1; Hearing loss, autosomal recessive; Retinal dystrophy; CDH23-related disorder	germline	19	Jan 12, 2026	clinvar