RS730882067 PRRT2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Infantile convulsions and choreoathetosis
Episodic kinesigenic dyskinesia
Episodic kinesigenic dyskinesia 1
PRRT2-associated paroxysmal movement disorder
Seizures
benign familial infantile
2
Episodic kinesigenic dyskinesia 1
Infantile convulsions and choreoathetosis
Episodic kinesigenic dyskinesia
Episodic kinesigenic dyskinesia 1
PRRT2-associated paroxysmal movement disorder
Seizures
benign familial infantile
2
Other Variants in PRRT2