Annotation Detail
Information
- Associated Genes
- RYR1
- Associated Variants
-
RYR1 p.Arg2241Gly (p.R2241G)
(
ENST00000355481.8,
ENST00000359596.8,
ENST00000689936.2,
ENST00000713952.1,
ENST00000713953.1 )
RYR1 p.Arg2241Gly (p.R2241G) ( ENST00000355481.8, ENST00000359596.8, ENST00000689936.2, ENST00000713952.1, ENST00000713953.1 ) - Associated Disease
- Malignant hyperthermia, susceptibility to, 1
- Source Database
- ClinVar
- Description
- NM_000540.3(RYR1):c.6721C>G (p.Arg2241Gly) AND Malignant hyperthermia, susceptibility to, 1
- ClinVar Allele ID
- 1929682
- ClinVar RefSeq Alternation Syntax
- NM_000540.3:c.6721C>G
- ClinVar RefSeq Alternation Syntax
- NM_001042723.2:c.6721C>G
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-03-23
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004009497
- ClinVar Disease
- Malignant hyperthermia, susceptibility to, 1
- Observed Origin Sample
- germline
Drugs