RYR2 NM_001035.3(RYR2):c.2204-7C>G

CI-VAR-00006939Explore in graph →NM_001035.3:c.2204-7C>GClinVar 36738 rs147479514

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
36738	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Cardiomyopathy; Arrhythmogenic right ventricular dysplasia 2; Catecholaminergic polymorphic ventricular tachycardia 1; Cardiovascular phenotype; Catecholaminergic polymorphic ventricular tachycardia; Ovarian serous cystadenocarcinoma; Lung cancer; Gastric cancer; Thymoma; Familial cancer of breast; Uterine corpus endometrial carcinoma	germline	21	Jun 01, 2026	clinvar