List of variants in gene VCL reported as uncertain significance for long QT syndrome

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_014000.3(VCL):c.2006G>A (p.Arg669Gln)	rs759771302	0.00003
NM_014000.3(VCL):c.565G>A (p.Val189Met)	rs151045204

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