List of variants reported as uncertain significance for Arrhythmogenic right ventricular dysplasia 1; Rienhoff syndrome

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_003239.5(TGFB3):c.-547dup	rs886050802	0.00013
NM_003239.5(TGFB3):c.1169A>T (p.Tyr390Phe)	rs996297395	0.00013
NM_003239.5(TGFB3):c.757G>A (p.Val253Met)	rs532517095	0.00011
NM_003239.5(TGFB3):c.97G>A (p.Gly33Ser)	rs781353815	0.00007
NM_003239.5(TGFB3):c.235C>G (p.Leu79Val)	rs371230847	0.00006
NM_003239.5(TGFB3):c.-30G>A	rs770828281	0.00004
NM_003239.5(TGFB3):c.850C>T (p.Pro284Ser)	rs1018415204	0.00004
NM_003239.5(TGFB3):c.872C>T (p.Pro291Leu)	rs145121701	0.00004
NM_003239.5(TGFB3):c.859C>T (p.Arg287Trp)	rs757774610	0.00003
NM_003239.5(TGFB3):c.82A>C (p.Thr28Pro)	rs564013964	0.00002
NM_003239.5(TGFB3):c.908A>C (p.Asp303Ala)	rs768423844	0.00002
NM_003239.5(TGFB3):c.1A>G (p.Met1Val)	rs375153534	0.00001
NM_003239.5(TGFB3):c.230G>A (p.Arg77Gln)	rs1036545575	0.00001
NM_003239.5(TGFB3):c.463C>T (p.Arg155Trp)	rs868258653	0.00001
NM_003239.5(TGFB3):c.487C>T (p.Arg163Trp)	rs142601521	0.00001
NM_003239.5(TGFB3):c.50T>G (p.Phe17Cys)	rs776354980	0.00001
NM_003239.5(TGFB3):c.580C>T (p.Arg194Trp)	rs368004396	0.00001
NM_003239.5(TGFB3):c.77C>G (p.Thr26Ser)	rs771543236	0.00001
NM_003239.5(TGFB3):c.-440CTT[2]	rs774422953
NM_003239.5(TGFB3):c.-536del	rs71451199
NM_003239.5(TGFB3):c.1219A>G (p.Lys407Glu)	rs1248127840
NM_003239.5(TGFB3):c.260G>T (p.Arg87Met)	rs1379970824
NM_003239.5(TGFB3):c.352+124C>G	rs977244423
NM_003239.5(TGFB3):c.464G>A (p.Arg155Gln)	rs925224125
NM_003239.5(TGFB3):c.756C>T (p.Gly252=)	rs369435862
NM_003239.5(TGFB3):c.965T>C (p.Ile322Thr)	rs762643638

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