RS141268327 SCN9A
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Associated Conditions
Severe myoclonic epilepsy in infancy
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Paroxysmal extreme pain disorder
Neuropathy
hereditary sensory and autonomic
type 2A
Primary erythromelalgia
Generalized epilepsy with febrile seizures plus
type 7
Inborn genetic diseases
Hereditary ataxia
Severe myoclonic epilepsy in infancy
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Other Variants in SCN9A