ClinVar Miner

List of variants in gene KCNQ1 reported as uncertain significance by Genetics and Molecular Pathology, SA Pathology

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.187C>T (p.Pro63Ser)	rs1280717988	0.00002
NM_000218.3(KCNQ1):c.1106C>T (p.Pro369Leu)	rs781369724

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