RS80356473 SCN9A

Health Risk Chr 2:166278156
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Primary erythromelalgia
Primary erythromelalgia
Other Variants in SCN9A
rs80356475 rs80356474 rs80356470 rs80356478 rs121908908 rs1574856736 rs121908909 rs121908910 rs121908911 rs121908912
Ask Dr. Hemsworth about this variant