RS387907127 PRRT2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Episodic kinesigenic dyskinesia 1
Infantile convulsions and choreoathetosis
Inborn genetic diseases
Episodic kinesigenic dyskinesia 1
Infantile convulsions and choreoathetosis
Inborn genetic diseases
Other Variants in PRRT2