CDH23 NM_022124.6(CDH23):c.7823G>A (p.Arg2608His)

CI-VAR-00008701Explore in graph →p.Arg2608HisNM_022124.6:c.7823G>AClinVar 46040 rs202052174

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
46040	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Retinitis pigmentosa-deafness syndrome; Neurodevelopmental abnormality; Usher syndrome type 1D; Autosomal recessive nonsyndromic hearing loss 12; Pituitary adenoma 5, multiple types; Rare genetic deafness; Retinal dystrophy	germline	19	Jan 25, 2026	clinvar