RS368820286 ALDH7A1

Health Risk Chr 5:126549924
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Pyridoxine-dependent epilepsy
Epilepsy
Inborn genetic diseases
Pyridoxine-dependent epilepsy
Epilepsy
Other Variants in ALDH7A1
rs121912707 rs121912708 rs779494572 rs1561672504 rs121912709 rs387906574 rs121912710 rs121912711 rs201948406 rs794727058
Ask Dr. Hemsworth about this variant