RS1018959938 SCN9A

Health Risk Chr 2:166242653
Upload your DNA to see your genotype for this variant.
Associated Conditions
Primary erythromelalgia
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Paroxysmal extreme pain disorder
Generalized epilepsy with febrile seizures plus
type 7
Neuropathy
hereditary sensory and autonomic
type 2A
Primary erythromelalgia
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Paroxysmal extreme pain disorder
Generalized epilepsy with febrile seizures plus
type 7
Other Variants in SCN9A
rs80356475 rs80356474 rs80356470 rs80356478 rs121908908 rs1574856736 rs121908909 rs121908910 rs121908911 rs121908912
Ask Dr. Hemsworth about this variant