List of variants in gene DSG2 reported as uncertain significance by Molecular Genetics Laboratory - Cardiogenetics, CHU de Nantes

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	gnomAD frequency
NM_001943.5(DSG2):c.1014+7A>G	rs756562276	0.00002
NM_001943.5(DSG2):c.82-1G>A	rs746353565	0.00001
NM_001943.5(DSG2):c.323C>G (p.Thr108Ser)	rs1284705376
NM_001943.5(DSG2):c.829-3C>A	rs1295936995

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