RS121908908 SCN9A

Health Risk Chr 2:166286562
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What This Variant Does
"rs121908908, also known as c.1376C&gt
Associated Conditions
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Channelopathy-associated congenital insensitivity to pain
autosomal recessive
Other Variants in SCN9A
rs80356475 rs80356474 rs80356470 rs80356478 rs1574856736 rs121908909 rs121908910 rs121908911 rs121908912 rs121908913
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