PCDH15 NM_001384140.1(PCDH15):c.475-3C>T

CI-VAR-00008715Explore in graph →NM_001384140.1:c.475-3C>TClinVar 46485 rs41304641

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
46485	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Usher syndrome type 1; Usher syndrome type 1F; Familial cancer of breast; Ovarian serous cystadenocarcinoma; Cholangiocarcinoma; Clear cell carcinoma of kidney; Sarcoma; Gastric cancer; Thymoma; Lung cancer	germline	11	Jun 01, 2026	clinvar