RS199986805 SCN9A

Health Risk Chr 2:166288543
Upload your DNA to see your genotype for this variant.
Associated Conditions
Paroxysmal extreme pain disorder
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Primary erythromelalgia
Neuropathy
hereditary sensory and autonomic
type 2A
Generalized epilepsy with febrile seizures plus
type 7
Paroxysmal extreme pain disorder
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Primary erythromelalgia
Neuropathy
hereditary sensory and autonomic
Other Variants in SCN9A
rs80356475 rs80356474 rs80356470 rs80356478 rs121908908 rs1574856736 rs121908909 rs121908910 rs121908911 rs121908912
Ask Dr. Hemsworth about this variant