RS759003928 SCN9A

Health Risk Chr 2:166242647
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Associated Conditions
Primary erythromelalgia
Paroxysmal extreme pain disorder
See cases
Inborn genetic diseases
Neuropathy
hereditary sensory and autonomic
type 2A
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Primary erythromelalgia
Paroxysmal extreme pain disorder
See cases
Inborn genetic diseases
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