RS397514737 GABRG2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Generalized epilepsy with febrile seizures plus 3
Self-limited epilepsy with centrotemporal spikes
EPILEPSY
CHILDHOOD ABSENCE
SUSCEPTIBILITY TO
2
Febrile seizures
familial
8
Developmental and epileptic encephalopathy
74
Inborn genetic diseases
Generalized epilepsy with febrile seizures plus 3
Self-limited epilepsy with centrotemporal spikes
EPILEPSY
Other Variants in GABRG2