RS118192170 RYR1
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What This Variant Does
"rs118192170, aka p.Ile4898Thr or p.I4898T, is a SNP in the RYR1 gene associated with both malignant ...
Associated Conditions
Central core myopathy
Malignant hyperthermia
susceptibility to
1
RYR1-related disorder
Congenital myopathy with fiber type disproportion
Congenital multicore myopathy with external ophthalmoplegia
halothane response - Toxicity
methoxyflurane response - Toxicity
succinylcholine response - Toxicity
desflurane response - Toxicity
enflurane response - Toxicity
isoflurane response - Toxicity
sevoflurane response - Toxicity
Congenital myopathy
Other Variants in RYR1