List of variants in gene DSG2 reported as uncertain significance for Dilated cardiomyopathy 1BB

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001943.5(DSG2):c.2328C>A (p.Phe776Leu)	rs771104668	0.00004
NM_001943.5(DSG2):c.3167C>T (p.Thr1056Ile)	rs767538450	0.00004
NM_001943.5(DSG2):c.1163T>G (p.Phe388Cys)	rs369214871	0.00001
NM_001943.5(DSG2):c.1525G>A (p.Asp509Asn)	rs753406968	0.00001
NM_001943.5(DSG2):c.373T>C (p.Phe125Leu)

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