SCN1A Chromosome 2

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

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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
RS1553532582 Health Risk Likely pathogenic
RS1553532782 Health Risk Likely pathogenic
RS1553534233 Health Risk Likely pathogenic
RS1553540464 Health Risk Likely pathogenic
RS1553540503 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE, Early-infantile DEE
RS1553541028 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1553541066 Health Risk Likely pathogenic
RS1553541172 Health Risk Likely pathogenic Early-infantile DEE, Seizure, Early-infantile DEE
RS1553541303 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Developmental and epileptic encephalopathy
RS1553541464 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS1553542262 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS1553543148 Health Risk Likely pathogenic
RS1553544470 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1553545740 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1553547403 Health Risk Likely pathogenic
RS1553549834 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, Developmental and epileptic encephalopathy
RS1553549845 Health Risk Likely pathogenic
RS1553549902 Health Risk Likely pathogenic
RS1553550552 Health Risk Likely pathogenic
RS1553551312 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE, Early-infantile DEE
RS1553551483 Health Risk Likely pathogenic
RS1553553593 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1553553614 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, Developmental and epileptic encephalopathy
RS1553560677 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, Early-infantile DEE, Developmental and epileptic encephalopathy
RS1553560710 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1553560740 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1553560766 Health Risk Likely pathogenic Sudden unexplained death in childhood, Sudden unexplained death in childhood
RS1559106126 Health Risk Likely pathogenic Developmental and epileptic encephalopathy 6B, Developmental and epileptic encephalopathy 6B
RS1559114202 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1559118914 Health Risk Likely pathogenic Autosomal dominant epilepsy, Autosomal dominant epilepsy
RS1559128483 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS1559140155 Health Risk Likely pathogenic Developmental and epileptic encephalopathy 6B, Developmental and epileptic encephalopathy 6B
RS1559149128 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, Severe myoclonic epilepsy in infancy, Early-infantile DEE
RS1559195296 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1559199628 Health Risk Likely pathogenic Lung cancer, Early-infantile DEE, Developmental and epileptic encephalopathy 6B
RS1559200901 Health Risk Likely pathogenic Inborn genetic diseases, Developmental and epileptic encephalopathy 6B, Early-infantile DEE
RS1559238215 Health Risk Likely pathogenic Generalized epilepsy with febrile seizures plus, type 2, Generalized epilepsy with febrile seizures plus
RS1559238432 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1573947939 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1573948129 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1573950349 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1573953030 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Severe myoclonic epilepsy in infancy
RS1573962628 Health Risk Likely pathogenic
RS1573964264 Health Risk Likely pathogenic Early-infantile DEE, Early-infantile DEE
RS1573984110 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Early-infantile DEE, Severe myoclonic epilepsy in infancy
RS1573991676 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Inborn genetic diseases, Severe myoclonic epilepsy in infancy
RS1574005699 Health Risk Likely pathogenic Severe myoclonic epilepsy in infancy, Severe myoclonic epilepsy in infancy
RS1574006857 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, Developmental and epileptic encephalopathy 6B, Developmental and epileptic encephalopathy
RS1574069096 Health Risk Likely pathogenic
RS1574172286 Health Risk Likely pathogenic
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