List of variants in gene DSG2 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_001943.5(DSG2):c.1814A>T (p.Asp605Val)	rs761157959	0.00001
NM_001943.5(DSG2):c.2664C>A (p.Phe888Leu)	rs773831600	0.00001

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