List of variants in gene SCN5A reported as 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.1673A>G (p.His558Arg)	rs1805124	0.24768
NM_000335.5(SCN5A):c.1571C>A (p.Ser524Tyr)	rs41313691	0.01184
NM_000335.5(SCN5A):c.3575G>A (p.Arg1192Gln)	rs41261344	0.00222
NM_000335.5(SCN5A):c.1715C>A (p.Ala572Asp)	rs36210423

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