RS121908911 SCN9A

Health Risk Chr 2:166228971
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Paroxysmal extreme pain disorder
Paroxysmal extreme pain disorder
Other Variants in SCN9A
rs80356475 rs80356474 rs80356470 rs80356478 rs121908908 rs1574856736 rs121908909 rs121908910 rs121908912 rs121908913
Ask Dr. Hemsworth about this variant