RS141686175 SCN11A
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What This Variant Does
"CLNSIG=5
Associated Conditions
Familial episodic pain syndrome with predominantly lower limb involvement
Hereditary sensory and autonomic neuropathy type 7
Inborn genetic diseases
Familial episodic pain syndrome with predominantly lower limb involvement
Hereditary sensory and autonomic neuropathy type 7
Inborn genetic diseases
Other Variants in SCN11A