List of variants in gene KCNQ2 reported as likely benign for electroclinical 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_172107.4(KCNQ2):c.1887+17G>A	rs369457896	0.00091
NM_172107.4(KCNQ2):c.691-14C>T	rs200448016	0.00004
NM_172107.4(KCNQ2):c.1997C>T (p.Pro666Leu)	rs762130930

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