RS11556732 PRRT2

Health Risk Chr 16:29813186 snv missense variant
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Associated Conditions
Episodic kinesigenic dyskinesia
Inborn genetic diseases
PRRT2-related disorder
Episodic kinesigenic dyskinesia
Inborn genetic diseases
PRRT2-related disorder
Population Frequencies
gnomAD ALL
0%
1kG AFR
99.6%
1kG ALL
0.1%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in PRRT2
rs730882065 rs730882066 rs730882067 rs387907125 rs1596893185 rs387907126 rs730882068 rs387907127 rs387907128 rs587778771
Ask Dr. Hemsworth about this variant