RS193922810 RYR1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=1
Associated Conditions
Malignant hyperthermia
susceptibility to
1
RYR1-related disorder
Malignant hyperthermia of anesthesia
Congenital multicore myopathy with external ophthalmoplegia
King Denborough syndrome
Central core myopathy
Autosomal dominant and autosomal recessive RYR1-related disorders
RYR1-related disorder
Congenital myopathy with fiber type disproportion
Malignant hyperthermia
susceptibility to
1
Malignant hyperthermia
Other Variants in RYR1