RS118192178 RYR1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Central core myopathy
RYR1-related disorder
Inborn genetic diseases
Congenital myopathy with fiber type disproportion
Abnormality of the musculature
King Denborough syndrome
Malignant hyperthermia
susceptibility to
1
Malignant hyperthermia
susceptibility to
1
RYR1-related myopathy
Congenital multicore myopathy with external ophthalmoplegia
Central core myopathy
Other Variants in RYR1