List of variants in gene combination KCNQ1, KCNQ1OT1 reported as uncertain significance for heart conduction disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.1456G>A (p.Ala486Thr)	rs753256800	0.00004
NM_000218.3(KCNQ1):c.1514+3G>A	rs374767819	0.00003
NM_000218.3(KCNQ1):c.1501A>G (p.Thr501Ala)	rs749196110	0.00001
NM_000218.3(KCNQ1):c.1514+9C>T	rs770840921	0.00001
NM_000218.3(KCNQ1):c.1394-13A>G	rs747187696

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