List of variants in gene KCNQ1 reported as uncertain significance by Molecular Genetics Laboratory - Cardiogenetics, CHU de Nantes

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.1532G>A (p.Arg511Gln)	rs753962384	0.00001
NM_000218.3(KCNQ1):c.1876G>A (p.Gly626Ser)	rs199472821	0.00001
NM_000218.3(KCNQ1):c.1128+4dup	rs2493701056
NM_000218.3(KCNQ1):c.584_604+46del	rs2493668013
NM_000218.3(KCNQ1):c.859G>T (p.Ala287Ser)	rs765665086

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