RYR2 NM_001035.3(RYR2):c.1864G>A (p.Gly622Arg)

CI-VAR-00155640Explore in graph →p.Gly622ArgNM_001035.3:c.1864G>AClinVar 923549 rs376243998

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
923549	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Cardiomyopathy; Arrhythmogenic right ventricular dysplasia 2; Catecholaminergic polymorphic ventricular tachycardia 1; Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome; Catecholaminergic polymorphic ventricular tachycardia; Uterine corpus endometrial carcinoma; Cardiovascular phenotype	germline	6	Jun 11, 2026	clinvar