RS587784491 TUBA1A
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Lissencephaly due to TUBA1A mutation
Inborn genetic diseases
Tubulinopathy
Decreased head circumference
Seizure
Global developmental delay
Neurodevelopmental disorder
Tubulinopathy-associated dysgyria
TUBA1A-related disorder
Lissencephaly due to TUBA1A mutation
Inborn genetic diseases
Tubulinopathy
Decreased head circumference
Seizure
Global developmental delay
Other Variants in TUBA1A