RYR1 NM_000540.3(RYR1):c.985G>A (p.Asp329Asn)

CI-VAR-00210416Explore in graph →p.Asp329AsnNM_000540.3:c.985G>AClinVar 1430036 rs1966919745

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
1430036	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	RYR1-related disorder; King Denborough syndrome; Congenital multicore myopathy with external ophthalmoplegia; Central core myopathy; Congenital myopathy with fiber type disproportion; Malignant hyperthermia, susceptibility to, 1; Inborn genetic diseases	germline	4	Dec 30, 2025	clinvar