List of variants in gene DSG2 reported as likely benign for Arrhythmogenic right ventricular cardiomyopathy

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001943.5(DSG2):c.1543G>A (p.Val515Ile)	rs2230235	0.00917
NM_001943.5(DSG2):c.473T>G (p.Val158Gly)	rs191143292	0.00550
NM_001943.5(DSG2):c.1174G>A (p.Val392Ile)	rs193922639	0.00158
NM_001943.5(DSG2):c.166G>A (p.Val56Met)	rs121913013	0.00150
NM_001943.5(DSG2):c.1003A>G (p.Thr335Ala)	rs191564916	0.00060
NM_001943.5(DSG2):c.1592T>G (p.Phe531Cys)	rs200484060	0.00001
NM_001943.5(DSG2):c.1714_1715dup	rs10645928
NM_001943.5(DSG2):c.*601TG[7]	rs36022761
NM_001943.5(DSG2):c.*944dup	rs368604939
NM_001943.5(DSG2):c.*960dup	rs200149790

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