RS193922837 RYR1
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What This Variant Does
"CLNSIG=5
Associated Conditions
RYR1-related disorder
Inborn genetic diseases
King Denborough syndrome
Central core myopathy
Malignant hyperthermia
susceptibility to
1
Myopathy
RYR1-associated
Centronuclear myopathy
Congenital multicore myopathy with external ophthalmoplegia
RYR1-related myopathy
RYR1-related disorder
Inborn genetic diseases
King Denborough syndrome
Other Variants in RYR1