RS776697656 RYR1
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Associated Conditions
Inborn genetic diseases
RYR1-related disorder
Central core myopathy
Congenital multicore myopathy with external ophthalmoplegia
Congenital myopathy with fiber type disproportion
Malignant hyperthermia
susceptibility to
1
King Denborough syndrome
RYR1-related myopathy
Inborn genetic diseases
RYR1-related disorder
Central core myopathy
Congenital multicore myopathy with external ophthalmoplegia
Congenital myopathy with fiber type disproportion
Other Variants in RYR1