RS121908918 SCN9A
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What This Variant Does
"[OMIM:?]
Associated Conditions
Generalized epilepsy with febrile seizures plus
type 7
Neuropathy
hereditary sensory and autonomic
type 2A
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Paroxysmal extreme pain disorder
Primary erythromelalgia
Inborn genetic diseases
Generalized epilepsy with febrile seizures plus
type 7
Neuropathy
hereditary sensory and autonomic
type 2A
Other Variants in SCN9A