RS118192150 RYR1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Central core myopathy
RYR1-related disorder
Congenital multicore myopathy with external ophthalmoplegia
Congenital myopathy with fiber type disproportion
Malignant hyperthermia
susceptibility to
1
King Denborough syndrome
Central core myopathy
RYR1-related disorder
Congenital multicore myopathy with external ophthalmoplegia
Congenital myopathy with fiber type disproportion
Malignant hyperthermia
susceptibility to
1
Other Variants in RYR1