RS368874586 RYR1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
RYR1-related disorder
Central core myopathy
Malignant hyperthermia of anesthesia
Congenital multicore myopathy with external ophthalmoplegia
Malignant hyperthermia
susceptibility to
1
RYR1-related disorder
Inborn genetic diseases
RYR1-related disorder
Central core myopathy
Malignant hyperthermia of anesthesia
Congenital multicore myopathy with external ophthalmoplegia
Malignant hyperthermia
Other Variants in RYR1