RS794726860 SLC6A1

Health Risk Chr 3:11025786
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Epilepsy with myoclonic atonic seizures
Autism spectrum disorder
Inborn genetic diseases
Epilepsy with myoclonic atonic seizures
Autism spectrum disorder
Other Variants in SLC6A1
rs144322561 rs794726859 rs876657400 rs749240316 rs876657401 rs886042046 rs1057524158 rs896013015 rs1057523845 rs1064795392
Ask Dr. Hemsworth about this variant