List of variants reported as uncertain significance for Arrhythmogenic right ventricular dysplasia 10 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001943.5(DSG2):c.1003A>G (p.Thr335Ala)	rs191564916	0.00060
NM_001943.5(DSG2):c.3095C>T (p.Thr1032Ile)	rs775546937	0.00005
NM_001943.5(DSG2):c.1885C>T (p.Pro629Ser)	rs200804638	0.00004
NM_001943.5(DSG2):c.3039C>A (p.Tyr1013Ter)	rs539821357	0.00003
NM_001943.5(DSG2):c.991G>A (p.Glu331Lys)	rs121913012	0.00002
NM_001943.5(DSG2):c.1035GAA[1] (p.Lys346del)	rs727502987
NM_001943.5(DSG2):c.1447G>A (p.Gly483Ser)	rs886053714
NM_001943.5(DSG2):c.3036_3037insG (p.Tyr1013fs)	rs2073310848
NM_001943.5(DSG2):c.3077G>A (p.Ser1026Asn)
NM_001943.5(DSG2):c.877A>T (p.Ile293Leu)	rs2230234

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