RYR1 Chromosome 19

Ryanodine receptor 1
1315 variants 24 Drug Response 1291 Health Risk

Upload your DNA to see your personal genotypes for variants in RYR1.

What This Gene Does
This gene encodes a ryanodine receptor found in skeletal muscle. The encoded protein functions as a calcium release channel in the sarcoplasmic reticulum but also serves to connect the sarcoplasmic reticulum and transverse tubule. Mutations in this gene are associated with malignant hyperthermia susceptibility, central core disease, and minicore myopathy with external ophthalmoplegia. Alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Ryanodine receptors|Protein phosphatase 1 regulatory subunits"
Locus Type
gene with protein product
Location
19q13.2
Ensembl
ENSG00000196218
Associated Conditions (74)
Central core myopathy
RYR1-related disorder
King Denborough syndrome
desflurane response - Toxicity
halothane response - Toxicity
enflurane response - Toxicity
isoflurane response - Toxicity
methoxyflurane response - Toxicity
sevoflurane response - Toxicity
succinylcholine response - Toxicity
RYR1-related myopathy
Malignant hyperthermia
susceptibility to
1
Congenital multicore myopathy with external ophthalmoplegia
Malignant hyperthermia of anesthesia
Congenital myopathy with fiber type disproportion
Inborn genetic diseases
Congenital myopathy
Myopathy
+54 more conditions
Key Variants
RS118192124
Likely pathogenic; drug response
Central core myopathy, RYR1-related disorder, King Denborough syndrome
Drug Response
RS121918596
Likely pathogenic; drug response
Malignant hyperthermia, susceptibility to, 1
Drug Response
RS193922748
Likely pathogenic; drug response
RYR1-related disorder, sevoflurane response - Toxicity, Malignant hyperthermia
Drug Response
RS193922762
Likely pathogenic; drug response
Malignant hyperthermia, susceptibility to, 1
Drug Response
RS193922770
Likely pathogenic; drug response
RYR1-related disorder, desflurane response - Toxicity, halothane response - Toxicity
Drug Response
RS193922818
Likely pathogenic; drug response
RYR1-related disorder, Malignant hyperthermia, susceptibility to
Drug Response
RS193922832
Likely pathogenic; drug response
RYR1-related disorder, sevoflurane response - Toxicity, desflurane response - Toxicity
Drug Response
RS193922876
Likely pathogenic; drug response
desflurane response - Toxicity, enflurane response - Toxicity, succinylcholine response - Toxicity
Drug Response
RS193922878
Likely pathogenic; drug response
desflurane response - Toxicity, halothane response - Toxicity, isoflurane response - Toxicity
Drug Response
RS28933397
Likely pathogenic; drug response
Malignant hyperthermia, susceptibility to, 1
Drug Response
RS118192122
Pathogenic; drug response
Central core myopathy, Malignant hyperthermia, susceptibility to
Drug Response
RS118192161
Pathogenic; drug response
Malignant hyperthermia, susceptibility to, 1
Drug Response
All Variants (1315)
RSID Category Clinical Significance Conditions
RS113812662 Health Risk Likely pathogenic Malignant hyperthermia, susceptibility to, 1
RS1161929108 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related disorder
RS1163185721 Health Risk Likely pathogenic Central core myopathy, Central core myopathy
RS1165213387 Health Risk Likely pathogenic Congenital multicore myopathy with external ophthalmoplegia, Congenital multicore myopathy with external ophthalmoplegia
RS117886618 Health Risk Likely pathogenic Malignant hyperthermia, susceptibility to, 1
RS118192117 Health Risk Likely pathogenic Congenital myopathy with fiber type disproportion, Central core myopathy, RYR1-related disorder
RS118192123 Health Risk Likely pathogenic Central core myopathy, RYR1-related disorder, Malignant hyperthermia
RS118192127 Health Risk Likely pathogenic Central core myopathy, RYR1-related disorder, Central core myopathy
RS118192140 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related disorder
RS118192146 Health Risk Likely pathogenic Central core myopathy, Central core myopathy, Central core myopathy
RS118192147 Health Risk Likely pathogenic Central core myopathy, RYR1-related disorder, Central core myopathy
RS118192148 Health Risk Likely pathogenic Central core myopathy, RYR1-related disorder, Inborn genetic diseases
RS118192151 Health Risk Likely pathogenic Central core myopathy, RYR1-related disorder, Congenital multicore myopathy with external ophthalmoplegia
RS118192153 Health Risk Likely pathogenic Central core myopathy, RYR1-related disorder, Central core myopathy
RS118192155 Health Risk Likely pathogenic Central core myopathy, RYR1-related disorder, RYR1-related disorder
RS118192162 Health Risk Likely pathogenic Malignant hyperthermia, susceptibility to, 1
RS118192163 Health Risk Likely pathogenic Malignant hyperthermia, susceptibility to, 1
RS118192168 Health Risk Likely pathogenic Congenital multicore myopathy with external ophthalmoplegia, Malignant hyperthermia, susceptibility to
RS118192171 Health Risk Likely pathogenic Neuromuscular disease, congenital, with uniform type 1 fiber
RS118192172 Health Risk Likely pathogenic Malignant hyperthermia, susceptibility to, 1
RS118192175 Health Risk Likely pathogenic Malignant hyperthermia, susceptibility to, 1
RS118192178 Health Risk Likely pathogenic Central core myopathy, RYR1-related disorder, Inborn genetic diseases
RS1185644472 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related disorder
RS1216966090 Health Risk Likely pathogenic RYR1-related disorder, Malignant hyperthermia, susceptibility to
RS1218605372 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related disorder
RS121918594 Health Risk Likely pathogenic Malignant hyperthermia, susceptibility to, 1
RS1228971728 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related disorder
RS1234999215 Health Risk Likely pathogenic Central core myopathy, RYR1-related disorder, Malignant hyperthermia
RS1238479593 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related myopathy, Malignant hyperthermia
RS1305053560 Health Risk Likely pathogenic Central core myopathy, Central core myopathy
RS1317181118 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related disorder
RS1354044963 Health Risk Likely pathogenic RYR1-related disorder, Malignant hyperthermia, susceptibility to
RS1387126664 Health Risk Likely pathogenic RYR1-related disorder, Malignant hyperthermia, susceptibility to
RS139161723 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related disorder
RS142929172 Health Risk Likely pathogenic RYR1-related disorder, Malignant hyperthermia, susceptibility to
RS1429521079 Health Risk Likely pathogenic Abnormality of the musculature, Abnormality of the musculature
RS1448949048 Health Risk Likely pathogenic RYR1-related disorder, Central core myopathy, Malignant hyperthermia
RS145087576 Health Risk Likely pathogenic Muscular dystrophy and arthrogryposis, Malignant hyperthermia, susceptibility to
RS146876145 Health Risk Likely pathogenic Malignant hyperthermia, susceptibility to, 1
RS148399313 Health Risk Likely pathogenic RYR1-related disorder, Malignant hyperthermia, susceptibility to
RS1555762532 Health Risk Likely pathogenic Rhabdomyolysis, Rhabdomyolysis
RS1555763657 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related disorder
RS1555769544 Health Risk Likely pathogenic
RS1555769818 Health Risk Likely pathogenic Distal arthrogryposis, Distal arthrogryposis
RS1555770968 Health Risk Likely pathogenic
RS1555777043 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related disorder
RS1555777086 Health Risk Likely pathogenic
RS1555779450 Health Risk Likely pathogenic
RS1555784801 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related disorder
RS1555785388 Health Risk Likely pathogenic RYR1-related disorder, RYR1-related disorder
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