SCN1A Chromosome 2

Sodium voltage-gated channel alpha subunit 1
1884 variants 1 Drug Response 1883 Health Risk

Upload your DNA to see your personal genotypes for variants in SCN1A.

What This Gene Does
Voltage-dependent sodium channels are heteromeric complexes that regulate sodium exchange between intracellular and extracellular spaces and are essential for the generation and propagation of action potentials in muscle cells and neurons. Each sodium channel is composed of a large pore-forming, glycosylated alpha subunit and two smaller beta subunits. This gene encodes a sodium channel alpha subunit, which has four homologous domains, each of which contains six transmembrane regions. Allelic variants of this gene are associated with generalized epilepsy with febrile seizures and epileptic encephalopathy. Alternative splicing results in multiple transcript variants. The RefSeq Project has decided to create four representative RefSeq records. Three of the transcript variants are supported by experimental evidence and the fourth contains alternate 5' untranslated exons, the exact combination of which have not been experimentally confirmed for the full-length transcript. [provided by RefSeq, Oct 2015]
Gene Info
Gene Group
Sodium voltage-gated channel alpha subunits
Locus Type
gene with protein product
Location
2q24.3
Ensembl
ENSG00000144285
Associated Conditions (56)
Febrile seizures
familial
3a
carbamazepine response - Dosage
Early-infantile DEE
Inborn genetic diseases
Developmental and epileptic encephalopathy 6B
Migraine
familial hemiplegic
3
Generalized epilepsy with febrile seizures plus
type 2
SCN1A-related disorder
type 1
Severe myoclonic epilepsy in infancy
Focal epilepsy
Autosomal dominant epilepsy
Seizure
Developmental and epileptic encephalopathy
Bilateral tonic-clonic seizure
+36 more conditions
Key Variants
All Variants (1884)
RSID Category Clinical Significance Conditions
RS1574183148 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Generalized epilepsy with febrile seizures plus, type 2
RS1574201555 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1574217232 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1574240716 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1574265485 Health Risk Likely pathogenic
RS1574266328 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS1574271644 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1574271827 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, Developmental and epileptic encephalopathy
RS1574282312 Health Risk Likely pathogenic
RS1574291210 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1574312497 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1684663181 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Severe myoclonic epilepsy in infancy
RS1684680680 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1689136140 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1689139851 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1689142827 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1689186812 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1689207347 Health Risk Likely pathogenic SCN1A-related channelopathy, SCN1A-related channelopathy
RS1689211960 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1689226880 Health Risk Likely pathogenic
RS1689240616 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE, Early-infantile DEE
RS1689280236 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Severe myoclonic epilepsy in infancy
RS1689294239 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1689298277 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1689298888 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1689350809 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE, Early-infantile DEE
RS1689377026 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1689381070 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1689981394 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1690003122 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1690013843 Health Risk Likely pathogenic Early-infantile DEE, Severe myoclonic epilepsy in infancy, Early-infantile DEE
RS1690331819 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1691026372 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS1691091949 Health Risk Likely pathogenic Migraine, familial hemiplegic, 3
RS1692543303 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, Developmental and epileptic encephalopathy
RS1692866593 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1696403356 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1697127484 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1697134047 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1697433995 Health Risk Likely pathogenic Migraine, familial hemiplegic, 3
RS1697647054 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1697904829 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, Developmental and epileptic encephalopathy
RS1697995660 Health Risk Likely pathogenic
RS1697998080 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1697998959 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, Developmental and epileptic encephalopathy
RS1697999557 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1698003832 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE, Early-infantile DEE
RS1698007004 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1698009615 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1698574524 Health Risk Likely pathogenic Migraine, familial hemiplegic, 3
« Prev 1 ... 7 8 9 10 11 12 13 ... 38 Next »
Sign Up to Analyze Your DNA Log In