RS77838305 PRRT2

Health Risk Chr 16:29813703
Upload your DNA to see your genotype for this variant.
Associated Conditions
Episodic kinesigenic dyskinesia
Infantile convulsions and choreoathetosis
Seizures
benign familial infantile
2
PRRT2-associated paroxysmal movement disorder
Episodic kinesigenic dyskinesia
Episodic kinesigenic dyskinesia
Infantile convulsions and choreoathetosis
Seizures
benign familial infantile
2
PRRT2-associated paroxysmal movement disorder
Episodic kinesigenic dyskinesia
Other Variants in PRRT2
rs730882065 rs730882066 rs730882067 rs387907125 rs1596893185 rs387907126 rs730882068 rs387907127 rs387907128 rs587778771
Ask Dr. Hemsworth about this variant