GABRA1 Chromosome 5

Gamma-aminobutyric acid type A receptor subunit alpha1
127 variants 127 Health Risk

Upload your DNA to see your personal genotypes for variants in GABRA1.

What This Gene Does
This gene encodes a gamma-aminobutyric acid (GABA) receptor. GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. GABA-A receptors are pentameric, consisting of proteins from several subunit classes: alpha, beta, gamma, delta and rho. Mutations in this gene cause juvenile myoclonic epilepsy and childhood absence epilepsy type 4. Multiple transcript variants encoding the same protein have been identified for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Gamma-aminobutyric acid type A receptor subunits
Locus Type
gene with protein product
Location
5q34
Ensembl
ENSG00000022355
Associated Conditions (14)
Epilepsy
idiopathic generalized
susceptibility to
13
childhood absence 4
Idiopathic generalized epilepsy
Developmental and epileptic encephalopathy
19
GABRA1-related disorder
Inborn genetic diseases
Intellectual disability
Epileptic encephalopathy
Juvenile myoclonic epilepsy
Intractable seizure
Key Variants
RS1064795283
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS1064796448
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS113886269
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS1312078830
Conflicting classifications of pathogenicity
GABRA1-related disorder, Inborn genetic diseases, GABRA1-related disorder
Health Risk
RS1313965409
Conflicting classifications of pathogenicity
Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
Health Risk
RS138259457
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS138671319
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS139163545
Conflicting classifications of pathogenicity
Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
Health Risk
RS139793542
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS142385746
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS143815396
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
RS144727170
Conflicting classifications of pathogenicity
Epilepsy, idiopathic generalized, susceptibility to
Health Risk
All Variants (127)
RSID Category Clinical Significance Conditions
RS1064795283 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS1064796448 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS113886269 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS1312078830 Health Risk Conflicting classifications of pathogenicity GABRA1-related disorder, Inborn genetic diseases, GABRA1-related disorder
RS1313965409 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS138259457 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS138671319 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS139163545 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS139793542 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS142385746 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS143815396 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS144727170 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS1457242041 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1554087620 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS1561587910 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS1581175017 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS1581220210 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS1754197638 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS1754199170 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS1755063375 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Developmental and epileptic encephalopathy, 19
RS1755333582 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS1755340949 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS1755409878 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS182930988 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS183280626 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 19, Developmental and epileptic encephalopathy
RS184629690 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS187522588 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS188133840 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS190024862 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS190043578 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS200218956 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, childhood absence 4
RS200750234 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS2113354062 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS2113381632 Health Risk Conflicting classifications of pathogenicity
RS2113381723 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS2532205020 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2532205137 Health Risk Conflicting classifications of pathogenicity Developmental and epileptic encephalopathy, 19, Epilepsy
RS2532239153 Health Risk Conflicting classifications of pathogenicity
RS2532261795 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, idiopathic generalized
RS2532280401 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS372742479 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS374616425 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS376693195 Health Risk Conflicting classifications of pathogenicity Idiopathic generalized epilepsy, Epilepsy, childhood absence 4
RS41303356 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS41308303 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS527890421 Health Risk Conflicting classifications of pathogenicity
RS541335259 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS543710675 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS551045474 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
RS564871157 Health Risk Conflicting classifications of pathogenicity Epilepsy, idiopathic generalized, susceptibility to
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