List of variants reported as likely benign for Catecholaminergic polymorphic ventricular tachycardia 5 by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.1538-13T>G	rs55704802	0.00651
NM_006073.4(TRDN):c.1567+19T>C	rs182813107	0.00419
NM_006073.4(TRDN):c.793+61T>C	rs572614305	0.00177
NM_006073.4(TRDN):c.1531C>A (p.Pro511Thr)	rs146935076	0.00170
NM_006073.4(TRDN):c.793+27G>A	rs189106156	0.00023
NM_006073.4(TRDN):c.1321+15A>G	rs373855431	0.00003
NM_006073.4(TRDN):c.485-7T>C	rs921833812	0.00002
NM_006073.4(TRDN):c.1672+6T>C	rs755974871	0.00001
NM_006073.4(TRDN):c.1721-4A>T	rs60743141
NM_006073.4(TRDN):c.425-11dup	rs950851610
NM_006073.4(TRDN):c.931+18del	rs201431159
NM_006073.4(TRDN):c.991+18C>T

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