Variants in gene combination KCNQ1, KCNQ1OT1 with conflicting interpretations reported as "uncertain significance and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.1459G>A (p.Glu487Lys)	rs1205552952	0.00015
NM_000218.3(KCNQ1):c.1456G>A (p.Ala486Thr)	rs753256800	0.00004
NM_000218.3(KCNQ1):c.1394-6C>A	rs759714698
NM_000218.3(KCNQ1):c.1394-8C>T	rs371488379

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