RS80356475 SCN9A

Health Risk Chr 2:166277251
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What This Variant Does
"[OMIM:?]
Associated Conditions
Primary erythromelalgia
Generalized epilepsy with febrile seizures plus
type 7
Neuropathy
hereditary sensory and autonomic
type 2A
Primary erythromelalgia
Generalized epilepsy with febrile seizures plus
type 7
Neuropathy
hereditary sensory and autonomic
type 2A
Other Variants in SCN9A
rs80356474 rs80356470 rs80356478 rs121908908 rs1574856736 rs121908909 rs121908910 rs121908911 rs121908912 rs121908913
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