List of variants reported as uncertain significance for Arrhythmogenic right ventricular dysplasia, familial, 14

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001792.5(CDH2):c.1306G>A (p.Asp436Asn)	rs142861371	0.00009
NM_001792.5(CDH2):c.1100C>T (p.Thr367Met)	rs200933425	0.00003
NM_001792.5(CDH2):c.1133A>G (p.Asn378Ser)	rs199977445	0.00003
NM_001792.5(CDH2):c.14C>T (p.Ala5Val)	rs1284853215	0.00003
NM_001792.5(CDH2):c.1604C>G (p.Thr535Ser)	rs546438155	0.00001
NM_020317.5(RSRP1):c.520+152_520+153insC

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