List of variants in gene KCNQ5 reported as likely pathogenic for not provided

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_019842.4(KCNQ5):c.2725C>T (p.Arg909Ter)	rs776643693	0.00001
NM_019842.4(KCNQ5):c.1075C>T (p.Arg359Cys)
NM_019842.4(KCNQ5):c.1248-3570T>C

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