RYR2 NM_001035.3(RYR2):c.14809-15C>G

CI-VAR-00006938Explore in graph →NM_001035.3:c.14809-15C>GClinVar 36735 rs790897

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
36735	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Cardiomyopathy; Catecholaminergic polymorphic ventricular tachycardia 1; Arrhythmogenic right ventricular dysplasia 2; Catecholaminergic polymorphic ventricular tachycardia; Thymoma; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Lung cancer; Familial cancer of breast	germline	20	May 01, 2026	clinvar