List of variants in gene DSG2 reported as likely benign by Illumina Laboratory Services, Illumina

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_001943.5(DSG2):c.2137G>A (p.Glu713Lys)	rs79241126	0.05477
NM_001943.5(DSG2):c.217-5G>T	rs80073511	0.01232
NM_001943.5(DSG2):c.3243C>T (p.Val1081=)	rs11542379	0.01097
NM_001943.5(DSG2):c.1543G>A (p.Val515Ile)	rs2230235	0.00917
NM_001943.5(DSG2):c.*677T>C	rs113622947	0.00882
NM_001943.5(DSG2):c.3135A>C (p.Thr1045=)	rs8095704	0.00801
NM_001943.5(DSG2):c.*1844A>G	rs16962096	0.00700
NM_001943.5(DSG2):c.2587A>C (p.Met863Leu)	rs16962093	0.00694
NM_001943.5(DSG2):c.*1385C>T	rs116439025	0.00624
NM_001943.5(DSG2):c.2759T>G (p.Val920Gly)	rs142841727	0.00439
NM_001943.5(DSG2):c.266A>G (p.Tyr89Cys)	rs2230232	0.00406
NM_001943.5(DSG2):c.*705G>A	rs57112788	0.00298
NM_001943.5(DSG2):c.*1674G>A	rs115630812	0.00261
NM_001943.5(DSG2):c.1051A>G (p.Ser351Gly)	rs139326669	0.00246
NM_001943.5(DSG2):c.*504A>G	rs139121154	0.00229
NM_001943.5(DSG2):c.3209C>T (p.Thr1070Met)	rs149617776	0.00223
NM_001943.5(DSG2):c.3295A>G (p.Thr1099Ala)	rs79068489	0.00137
NM_001943.5(DSG2):c.2368C>T (p.His790Tyr)	rs114544564	0.00130
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.*1071T>C	rs183684674	0.00012
NM_001943.5(DSG2):c.*1596T>C	rs549396103	0.00012
NM_001943.5(DSG2):c.1911C>T (p.Cys637=)	rs201654341	0.00004
NM_001943.5(DSG2):c.2906C>T (p.Ala969Val)	rs373598034	0.00004
NM_001943.5(DSG2):c.1303G>A (p.Asp435Asn)	rs370509593	0.00003
NM_001943.5(DSG2):c.1376A>G (p.Tyr459Cys)	rs576404380	0.00003
NM_001943.5(DSG2):c.*1471T>C	rs574977992	0.00002
NM_001943.5(DSG2):c.*238T>G	rs555035341	0.00002
NM_001943.5(DSG2):c.1914A>G (p.Gly638=)	rs200395484	0.00002
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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