RS766311956 PNPO

Health Risk Chr 17:47945594
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Pyridoxal phosphate-responsive seizures
Inborn genetic diseases
Pyridoxal phosphate-responsive seizures
Other Variants in PNPO
rs104894629 rs774710082 rs104894631 rs267606958 rs546737191 rs144362146 rs796052870 rs370243877 rs796052872 rs148597698
Ask Dr. Hemsworth about this variant