List of variants reported as uncertain significance for atrial fibrillation by New York Genome Center

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.1355G>A (p.Arg452Gln)	rs145229963	0.00025
NM_172201.2(KCNE2):c.80G>A (p.Arg27His)	rs148968498	0.00025
NM_000218.3(KCNQ1):c.1189C>T (p.Arg397Trp)	rs199472776	0.00013
NM_172201.2(KCNE2):c.369_370del (p.Ter124IleextTer?)	rs45610936	0.00009
NM_000335.5(SCN5A):c.5968C>T (p.Arg1990Trp)	rs371308670	0.00003
NM_000218.3(KCNQ1):c.1726G>A (p.Val576Ile)	rs750409379	0.00002
NM_000335.5(SCN5A):c.4168G>A (p.Gly1390Arg)	rs780405533	0.00002
NM_002476.2(MYL4):c.194G>A (p.Arg65Gln)	rs1050214578	0.00002
NM_153485.3(NUP155):c.1348A>G (p.Met450Val)	rs374935918	0.00002
NM_000218.3(KCNQ1):c.506C>T (p.Thr169Met)	rs199472693	0.00001
NM_000218.3(KCNQ1):c.1090T>C (p.Phe364Leu)
NM_000218.3(KCNQ1):c.1924T>C (p.Cys642Arg)	rs1410404016
NM_000218.3(KCNQ1):c.285C>G (p.Ser95Arg)
NM_002234.4(KCNA5):c.10G>T (p.Ala4Ser)
NM_006393.3(NEBL):c.1228-1338del	rs1841465820

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