List of variants reported as pathogenic for atrial fibrillation by Fulgent Genetics, Fulgent Genetics

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		ClinVar version:

Total variants: 32

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.673C>T (p.Arg225Trp)	rs199473072	0.00009
NM_000335.5(SCN5A):c.5869C>T (p.Arg1957Ter)	rs757532106	0.00004
NM_000218.3(KCNQ1):c.692G>A (p.Arg231His)	rs199472709	0.00003
NM_000335.5(SCN5A):c.1127G>A (p.Arg376His)	rs199473101	0.00003
NM_001037.5(SCN1B):c.363C>G (p.Cys121Trp)	rs104894718	0.00003
NM_001037.5(SCN1B):c.254G>A (p.Arg85His)	rs16969925	0.00002
NM_000218.3(KCNQ1):c.1085A>G (p.Lys362Arg)	rs12720458	0.00001
NM_000218.3(KCNQ1):c.1588C>T (p.Gln530Ter)	rs397508097	0.00001
NM_000218.3(KCNQ1):c.1615C>T (p.Arg539Trp)	rs199472795	0.00001
NM_000218.3(KCNQ1):c.1664G>A (p.Arg555His)	rs199472800	0.00001
NM_000218.3(KCNQ1):c.1781G>A (p.Arg594Gln)	rs199472815	0.00001
NM_000218.3(KCNQ1):c.521G>A (p.Arg174His)	rs199472697	0.00001
NM_000218.3(KCNQ1):c.674C>T (p.Ser225Leu)	rs199473456	0.00001
NM_000218.3(KCNQ1):c.914G>A (p.Trp305Ter)	rs120074186	0.00001
NM_000335.5(SCN5A):c.1099C>T (p.Arg367Cys)	rs199473097	0.00001
NM_000335.5(SCN5A):c.665G>A (p.Arg222Gln)	rs45546039	0.00001
NM_000218.3(KCNQ1):c.1014CTT[1] (p.Phe340del)	rs397508068
NM_000218.3(KCNQ1):c.1075C>T (p.Gln359Ter)	rs397508075
NM_000218.3(KCNQ1):c.1343dup (p.Glu449fs)	rs397508087
NM_000218.3(KCNQ1):c.513C>G (p.Tyr171Ter)	rs139042529
NM_000218.3(KCNQ1):c.796del (p.Leu266fs)	rs397508125
NM_000218.3(KCNQ1):c.805G>A (p.Gly269Ser)	rs120074193
NM_000218.3(KCNQ1):c.921+1G>T	rs397508130
NM_000335.5(SCN5A):c.2550_2551dup (p.Phe851fs)	rs397514450
NM_000335.5(SCN5A):c.4219G>A (p.Gly1407Arg)	rs137854612
NM_000335.5(SCN5A):c.4242+1G>C	rs794728879
NM_000335.5(SCN5A):c.4844TCT[1] (p.Phe1616del)	rs749697698
NM_000335.5(SCN5A):c.4864C>T (p.Arg1622Ter)	rs137854613
NM_000335.5(SCN5A):c.5414_5417del (p.Thr1805fs)	rs1060501127
NM_000335.5(SCN5A):c.664C>T (p.Arg222Ter)	rs794728849
NM_000891.3(KCNJ2):c.199C>T (p.Arg67Trp)	rs104894580
NM_000891.3(KCNJ2):c.653G>A (p.Arg218Gln)	rs199473384

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