List of variants in gene SCN5A reported as likely benign for atrial fibrillation

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.1381T>G (p.Leu461Val)	rs41313697	0.00352
NM_000335.5(SCN5A):c.1335C>T (p.His445=)	rs368045716	0.00048
NM_000335.5(SCN5A):c.5452G>A (p.Asp1818Asn)	rs137854619	0.00006
NM_000335.5(SCN5A):c.1557T>C (p.Ser519=)	rs371560571	0.00003
NM_000335.5(SCN5A):c.1677A>G (p.Thr559=)	rs376389170	0.00002
NM_000335.5(SCN5A):c.1992C>T (p.Ser664=)	rs368167264	0.00002
NM_000335.5(SCN5A):c.2694G>A (p.Glu898=)	rs2061655979	0.00001
NM_000335.5(SCN5A):c.786C>T (p.Ser262=)	rs753246399	0.00001
NM_000335.5(SCN5A):c.168G>A (p.Leu56=)	rs376742447
NM_000335.5(SCN5A):c.5848G>T (p.Val1950Leu)	rs41315493
NM_000335.5(SCN5A):c.795C>T (p.Ala265=)	rs527692731

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