RS200185692 SCN9A
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Associated Conditions
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Primary erythromelalgia
Paroxysmal extreme pain disorder
Neuropathy
hereditary sensory and autonomic
type 2A
Generalized epilepsy with febrile seizures plus
type 7
Inborn genetic diseases
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Primary erythromelalgia
Paroxysmal extreme pain disorder
Neuropathy
Other Variants in SCN9A