List of variants reported as likely pathogenic for Sinoatrial node dysfunction and deafness

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000720.4(CACNA1D):c.1127C>T (p.Ala376Val)	rs759274321	0.00003
NM_000720.4(CACNA1D):c.1208_1209insGGG (p.Gly403dup)	rs398122827
NM_001128840.3(CACNA1D):c.2248A>T (p.Ile750Phe)	rs1576484361
NM_001128840.3(CACNA1D):c.2907del (p.Phe970fs)

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