RS114854233 SCN11A

Health Risk Chr 3:38847190 snv missense variant

Upload your DNA to see your genotype for this variant.

Associated Conditions

Hereditary sensory and autonomic neuropathy type 7

Familial episodic pain syndrome with predominantly lower limb involvement

Inborn genetic diseases

Hereditary sensory and autonomic neuropathy type 7

Familial episodic pain syndrome with predominantly lower limb involvement

Inborn genetic diseases

Population Frequencies

gnomAD ALL

100%

1kG AFR

100%

1kG ALL

100%

1kG AMR

100%

1kG EAS

100%

1kG EUR

0.1%

1kG SAS

100%

Other Variants in SCN11A