List of variants in gene KCNQ1 reported as uncertain significance for Atrial fibrillation, familial, 3; Long QT syndrome 1; Jervell and Lange-Nielsen syndrome 1; Short QT syndrome type 2

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.1189C>T (p.Arg397Trp)	rs199472776	0.00013
NM_000218.3(KCNQ1):c.1726G>A (p.Val576Ile)	rs750409379	0.00002
NM_000218.3(KCNQ1):c.506C>T (p.Thr169Met)	rs199472693	0.00001
NM_000218.3(KCNQ1):c.1090T>C (p.Phe364Leu)
NM_000218.3(KCNQ1):c.1924T>C (p.Cys642Arg)	rs1410404016
NM_000218.3(KCNQ1):c.387-6394G>C
NM_000218.3(KCNQ1):c.899C>A (p.Ala300Glu)	rs1001293702

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