List of variants in gene SCN1B reported as likely pathogenic for atrial fibrillation

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001037.5(SCN1B):c.373C>T (p.Arg125Cys)	rs1135401736	0.00001
NM_001037.5(SCN1B):c.374G>A (p.Arg125His)	rs759839781	0.00001
NM_001037.5(SCN1B):c.448+201C>T	rs2151746638

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