List of variants in gene combination KCNQ1, KCNQ1OT1 reported as not provided for long QT syndrome

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_000218.3(KCNQ1):c.1430C>T (p.Pro477Leu)	rs199472784
NM_000218.3(KCNQ1):c.1513C>T (p.Gln505Ter)	rs397508091
NM_000218.3(KCNQ1):c.1514+1G>A	rs397508093

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