RS1064793851 PRRT2

Health Risk Chr 16:29813653
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What This Variant Does
"CLNSIG=5
Associated Conditions
Episodic kinesigenic dyskinesia
Inborn genetic diseases
Episodic kinesigenic dyskinesia
Inborn genetic diseases
Other Variants in PRRT2
rs730882065 rs730882066 rs730882067 rs387907125 rs1596893185 rs387907126 rs730882068 rs387907127 rs387907128 rs587778771
Ask Dr. Hemsworth about this variant