CDH23 NM_022124.6(CDH23):c.7849G>C (p.Gly2617Arg)

CI-VAR-00160736Explore in graph →p.Gly2617ArgNM_022124.6:c.7849G>CClinVar 944185 rs369379727

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
944185	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Autosomal recessive nonsyndromic hearing loss 12; Usher syndrome type 1D; Usher syndrome type 1; Pituitary adenoma 5, multiple types; Inborn genetic diseases	germline	10	Dec 25, 2024	clinvar