SCN2A Chromosome 2

Sodium voltage-gated channel alpha subunit 2
674 variants 674 Health Risk

Upload your DNA to see your personal genotypes for variants in SCN2A.

What This Gene Does
Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with four repeat domains, each of which is composed of six membrane-spanning segments, and one or more regulatory beta subunits. Voltage-gated sodium channels function in the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family. Allelic variants of this gene are associated with seizure disorders and autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]
Gene Info
Gene Group
Sodium voltage-gated channel alpha subunits
Locus Type
gene with protein product
Location
2q24.3
Ensembl
ENSG00000136531
Associated Conditions (57)
Seizures
benign familial infantile
3
Developmental and epileptic encephalopathy
11
Inborn genetic diseases
SCN2A-mediated disorder
Intellectual disability
Complex neurodevelopmental disorder
Episodic ataxia
type 9
Genetic developmental and epileptic encephalopathy
SCN2A-related disorder
See cases
Seizure
Pyridoxine-dependent epilepsy
Febrile seizure (within the age range of 3 months to 6 years)
Self-limited epilepsy with centrotemporal spikes
Hemiplegia/hemiparesis
Spastic ataxia
+37 more conditions
Key Variants
All Variants (674)
RSID Category Clinical Significance Conditions
RS2468008621 Health Risk Likely pathogenic benign sporadic neonatal-infantile epilepsy, benign sporadic neonatal-infantile epilepsy
RS2468035550 Health Risk Likely pathogenic Seizures, benign familial infantile, 3
RS2468035572 Health Risk Likely pathogenic Seizures, benign familial infantile, 3
RS2468035584 Health Risk Likely pathogenic SCN2A-related disorder, SCN2A-related disorder
RS2468061249 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468081746 Health Risk Likely pathogenic Neurodevelopmental delay, Neurodevelopmental delay
RS2468082494 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468096296 Health Risk Likely pathogenic Infantile spasms, Infantile spasms
RS2468102171 Health Risk Likely pathogenic Seizures, benign familial infantile, 3
RS2468102480 Health Risk Likely pathogenic Complex neurodevelopmental disorder, Complex neurodevelopmental disorder
RS2468102901 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468114101 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468126249 Health Risk Likely pathogenic Episodic ataxia, type 9, Developmental and epileptic encephalopathy
RS2468126672 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468126706 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Seizures
RS2468129385 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Seizures
RS2468129590 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468129607 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468129644 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468129879 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468149284 Health Risk Likely pathogenic Seizures, benign familial infantile, 3
RS2468149427 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468149509 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468149619 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Seizures
RS2468157518 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Seizures
RS2468157758 Health Risk Likely pathogenic Episodic ataxia, type 9, Episodic ataxia
RS2468157815 Health Risk Likely pathogenic unclassified developmental and epileptic encephalopathy, unclassified developmental and epileptic encephalopathy
RS2468158024 Health Risk Likely pathogenic Seizures, benign familial infantile, 3
RS2468158264 Health Risk Likely pathogenic
RS2468158340 Health Risk Likely pathogenic Seizures, benign familial infantile, 3
RS2468158869 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468158980 Health Risk Likely pathogenic benign sporadic infantile epilepsy, benign sporadic infantile epilepsy
RS2468159089 Health Risk Likely pathogenic Complex neurodevelopmental disorder, Developmental and epileptic encephalopathy, 11
RS2468159200 Health Risk Likely pathogenic SCN2A-related disorder, SCN2A-related disorder
RS2468159814 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS2468159922 Health Risk Likely pathogenic Seizures, benign familial infantile, 3
RS387906683 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Complex neurodevelopmental disorder
RS387906686 Health Risk Likely pathogenic Episodic ataxia, type 9, Seizures
RS75145688 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS768403673 Health Risk Likely pathogenic Seizures, benign familial infantile, 3
RS786205635 Health Risk Likely pathogenic
RS794727003 Health Risk Likely pathogenic
RS796053114 Health Risk Likely pathogenic
RS796053116 Health Risk Likely pathogenic
RS796053118 Health Risk Likely pathogenic Seizures, benign familial infantile, 3
RS796053119 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Developmental and epileptic encephalopathy
RS796053122 Health Risk Likely pathogenic Complex neurodevelopmental disorder, Complex neurodevelopmental disorder
RS796053124 Health Risk Likely pathogenic Developmental and epileptic encephalopathy, 11, Seizure
RS796053133 Health Risk Likely pathogenic
RS796053136 Health Risk Likely pathogenic
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