RS587777308 GABRA1

Health Risk Chr 5:161873196
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
19
Inborn genetic diseases
Idiopathic generalized epilepsy
Epilepsy
idiopathic generalized
susceptibility to
13
childhood absence 4
Developmental and epileptic encephalopathy
19
Inborn genetic diseases
Idiopathic generalized epilepsy
Epilepsy
idiopathic generalized
Other Variants in GABRA1
rs121434579 rs1581220270 rs138259457 rs587777307 rs587777309 rs587777363 rs587777364 rs76224028 rs138671319 rs144727170
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