List of variants in gene SCN5A reported as likely pathogenic 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.4475A>G (p.Lys1492Arg)	rs199473260	0.00004
NM_000335.5(SCN5A):c.1127G>A (p.Arg376His)	rs199473101	0.00003
NM_000335.5(SCN5A):c.3953G>T (p.Gly1318Val)	rs199473220	0.00003
NM_000335.5(SCN5A):c.1567C>T (p.Arg523Cys)	rs199473119	0.00001
NM_000335.5(SCN5A):c.4856C>T (p.Thr1619Met)	rs199473282	0.00001
NM_000335.5(SCN5A):c.5126C>T (p.Ser1709Leu)	rs137854604	0.00001
NM_000335.5(SCN5A):c.5224G>A (p.Gly1742Arg)	rs199473305	0.00001
NM_000335.5(SCN5A):c.310C>T (p.Arg104Trp)	rs199473055

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