List of variants studied for Brugada syndrome by New York Genome Center

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.266C>G (p.Ala89Gly)	rs200165636	0.00010
NM_000335.5(SCN5A):c.1654G>T (p.Gly552Trp)	rs3918389	0.00005
NM_000335.5(SCN5A):c.5968C>T (p.Arg1990Trp)	rs371308670	0.00003
NM_000719.7(CACNA1C):c.2486A>G (p.Asn829Ser)	rs773015884	0.00003
NM_000335.5(SCN5A):c.4168G>A (p.Gly1390Arg)	rs780405533	0.00002
NM_000719.7(CACNA1C):c.4141-605G>A	rs1054703481	0.00002
NM_005477.3(HCN4):c.1385G>A (p.Gly462Glu)	rs146714274	0.00002
NM_000335.5(SCN5A):c.5126C>T (p.Ser1709Leu)	rs137854604	0.00001
NM_001267550.2(TTN):c.95665G>A (p.Ala31889Thr)	rs1025105445	0.00001
NM_000256.3(MYBPC3):c.3764C>G (p.Ala1255Gly)	rs727504722
NM_000335.5(SCN5A):c.127C>T (p.Arg43Ter)	rs1553607597
NM_000719.7(CACNA1C):c.3577G>A (p.Ala1193Thr)	rs1251955384
NM_001267550.2(TTN):c.65143C>G (p.Arg21715Gly)	rs766522121
NM_005477.3(HCN4):c.1573C>T (p.Arg525Cys)	rs1429346819
NM_005477.3(HCN4):c.2504C>T (p.Ser835Phe)
Single allele

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