RS201948406 ALDH7A1

Health Risk Chr 5:126568296
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Pyridoxine-dependent epilepsy
Inborn genetic diseases
Seizure
ALDH7A1-related disorder
Pyridoxine-dependent epilepsy
Pyridoxine-dependent epilepsy
Inborn genetic diseases
Seizure
ALDH7A1-related disorder
Pyridoxine-dependent epilepsy
Other Variants in ALDH7A1
rs121912707 rs121912708 rs779494572 rs1561672504 rs121912709 rs387906574 rs121912710 rs121912711 rs794727058 rs375491094
Ask Dr. Hemsworth about this variant