RS138607170 SCN11A

Health Risk Chr 3:38925453 snv missense variant
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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
Population Frequencies
gnomAD ALL
100%
Other Variants in SCN11A
rs483352920 rs483352921 rs141686175 rs606231280 rs1050521607 rs1064795711 rs374524879 rs1085307142 rs767279633 rs201107889
Ask Dr. Hemsworth about this variant