List of variants in gene DSG2 reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 15

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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.3135A>C (p.Thr1045=)	rs8095704	0.00801
NM_001943.5(DSG2):c.2647T>C (p.Ser883Pro)	rs34417028	0.00652
NM_001943.5(DSG2):c.2708C>T (p.Thr903Ile)	rs34065672	0.00649
NM_001943.5(DSG2):c.473T>G (p.Val158Gly)	rs191143292	0.00550
NM_001943.5(DSG2):c.1051A>G (p.Ser351Gly)	rs139326669	0.00246
NM_001943.5(DSG2):c.3209C>T (p.Thr1070Met)	rs149617776	0.00223
NM_001943.5(DSG2):c.1652-12C>T	rs140850369	0.00173
NM_001943.5(DSG2):c.1174G>A (p.Val392Ile)	rs193922639	0.00158
NM_001943.5(DSG2):c.3295A>G (p.Thr1099Ala)	rs79068489	0.00137
NM_001943.5(DSG2):c.1875G>C (p.Leu625=)	rs35743180	0.00128
NM_001943.5(DSG2):c.2703A>G (p.Lys901=)	rs113591687	0.00114
NM_001943.5(DSG2):c.216+16G>A	rs200239610	0.00073
NM_001943.5(DSG2):c.1280+18G>C	rs141175168	0.00030
NM_001943.5(DSG2):c.1280+17C>T	rs199885701	0.00017

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