List of variants in gene TRDN reported as likely benign for catecholaminergic polymorphic ventricular tachycardia 5

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.1538-13T>G	rs55704802	0.00651
NM_006073.4(TRDN):c.793+61T>C	rs572614305	0.00177
NM_006073.4(TRDN):c.611-19A>T	rs142018848	0.00044
NM_006073.4(TRDN):c.367G>A (p.Asp123Asn)	rs201021891	0.00036
NM_006073.4(TRDN):c.1472-13C>T	rs367962513	0.00033
NM_006073.4(TRDN):c.23-19T>G	rs370102595	0.00011
NM_006073.4(TRDN):c.1975+8C>T	rs754046696	0.00006
NM_006073.4(TRDN):c.931+10T>A	rs754118635	0.00002
NM_006073.4(TRDN):c.502G>A (p.Glu168Lys)	rs545032318	0.00001
NM_006073.4(TRDN):c.1672+6T>C
NM_006073.4(TRDN):c.1721-4A>T	rs60743141
NM_006073.4(TRDN):c.233-14_233-13del	rs66509682
NM_006073.4(TRDN):c.425-11dup	rs950851610
NM_006073.4(TRDN):c.931+18del	rs201431159

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