RS121908916 SCN9A

Health Risk Chr 2:166303162
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What This Variant Does
"rs121908916, also known as c.829C&gt
Associated Conditions
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Generalized epilepsy with febrile seizures plus
type 7
Neuropathy
hereditary sensory and autonomic
type 2A
Inborn genetic diseases
Neuropathy
hereditary sensory and autonomic
type 2A
Generalized epilepsy with febrile seizures plus
type 7
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Other Variants in SCN9A
rs80356475 rs80356474 rs80356470 rs80356478 rs121908908 rs1574856736 rs121908909 rs121908910 rs121908911 rs121908912
Ask Dr. Hemsworth about this variant