RS17737379 TRDN

Health Risk Chr 6:123375620 snv missense variant

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Associated Conditions

Catecholaminergic polymorphic ventricular tachycardia 1

Cardiovascular phenotype

Catecholaminergic polymorphic ventricular tachycardia 1

Cardiovascular phenotype

Population Frequencies

gnomAD ALL

11.8%

1kG AFR

31.2%

1kG ALL

85.3%

1kG AMR

88%

1kG EAS

6.6%

1kG EUR

13.1%

1kG SAS

95.5%

Other Variants in TRDN