Variant · Snv
RYR1 NM_000540.3(RYR1):c.10347+1G>A
CI-VAR-00037172Explore in graph →NM_000540.3:c.10347+1G>AClinVar 224998 rs111436401
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.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 224998 | Pathogenic | reviewed by expert panel | 3 | Inborn genetic diseases; Congenital multicore myopathy with external ophthalmoplegia; Central core myopathy; Congenital myopathy with fiber type disproportion; Malignant hyperthermia, susceptibility to, 1; RYR1-related disorder; King Denborough syndrome; RYR1-related myopathy | germline | 12 | Sep 08, 2025 | clinvar |