List of variants in gene DSG2 reported as likely pathogenic for Cardiovascular phenotype

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001943.5(DSG2):c.2001+1G>T
NM_001943.5(DSG2):c.2434G>T (p.Gly812Cys)	rs121913010
NM_001943.5(DSG2):c.2617C>T (p.Gln873Ter)
NM_001943.5(DSG2):c.2620del (p.Thr874fs)	rs755243947
NM_001943.5(DSG2):c.2955del (p.Val986fs)	rs1064794709
NM_001943.5(DSG2):c.3059_3062del (p.Glu1020fs)	rs397516706
NM_001943.5(DSG2):c.523+1G>A	rs553299589
NM_001943.5(DSG2):c.523+1G>C	rs553299589

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