List of variants in gene DSG2 reported as uncertain significance for heart conduction disease

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.166G>A (p.Val56Met)	rs121913013	0.00150
NM_001943.5(DSG2):c.2623A>G (p.Met875Val)	rs370316475	0.00002

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