List of variants in gene combination KCNQ1, KCNQ1OT1 reported as uncertain significance for Jervell and Lange-Nielsen syndrome 1

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: 4

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HGVS	dbSNP
NM_000218.3(KCNQ1):c.1394-13A>G
NM_000218.3(KCNQ1):c.1394-8C>T	rs371488379
NM_181798.1(KCNQ1):c.1095A>G (p.Glu365=)	rs370676650
NM_181798.1(KCNQ1):c.1133+9C>T	rs770840921

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