RS587782996 PURA
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Seizure
Neonatal hypotonia
Intellectual disability
Global developmental delay
Delayed speech and language development
Abnormality of the nervous system
PURA-related disorder
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome
Seizure
Neonatal hypotonia
Intellectual disability
Global developmental delay
Delayed speech and language development
Abnormality of the nervous system
PURA-related disorder
Other Variants in PURA