List of variants reported as likely pathogenic for heart conduction disease by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.13528G>A (p.Ala4510Thr)	rs397516510
NM_001035.3(RYR2):c.37T>C (p.Phe13Leu)	rs794728761
NM_006073.4(TRDN):c.502G>T (p.Glu168Ter)	rs545032318
NM_006073.4(TRDN):c.550+1_550+2insA

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