List of variants in gene KCNQ1 reported as benign 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.*875A>G	rs8234	0.38150
NM_000218.3(KCNQ1):c.*932A>G	rs10798	0.37559
NM_000218.3(KCNQ1):c.1638G>A (p.Ser546=)	rs1057128	0.16286
NM_000218.3(KCNQ1):c.*479G>A	rs2519184	0.10424
NM_000218.3(KCNQ1):c.1590+14T>C	rs11024034	0.07860
NM_000218.3(KCNQ1):c.478-10G>A	rs28730752	0.04910
NM_000218.3(KCNQ1):c.1343C>G (p.Pro448Arg)	rs12720449
NM_000218.3(KCNQ1):c.1986C>T (p.Tyr662=)	rs11601907

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