List of variants in gene DSC2 reported as likely benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_024422.6(DSC2):c.2251-27C>A	rs151289743	0.01365
NM_024422.6(DSC2):c.2194T>G (p.Leu732Val)	rs151024019	0.00138
NM_024422.6(DSC2):c.304G>A (p.Glu102Lys)	rs144799937	0.00070
NM_024422.6(DSC2):c.1787C>T (p.Ala596Val)	rs148185335	0.00060
NM_024422.6(DSC2):c.270G>A (p.Glu90=)	rs138643506	0.00056
NM_024422.6(DSC2):c.1914G>C (p.Gln638His)	rs147742157	0.00036
NM_024422.6(DSC2):c.1559T>C (p.Ile520Thr)	rs561310777	0.00029
NM_024422.6(DSC2):c.348A>G (p.Gln116=)	rs137941742	0.00021
NM_024422.6(DSC2):c.907G>A (p.Val303Met)	rs145560678	0.00021
NM_024422.6(DSC2):c.1521-7C>T	rs374810953	0.00015
NM_024422.6(DSC2):c.397G>A (p.Ala133Thr)	rs200218585	0.00004
NM_024422.6(DSC2):c.870A>G (p.Pro290=)	rs142653119	0.00003
NM_024422.6(DSC2):c.1548G>T (p.Gly516=)	rs1465276759	0.00001
NM_024422.6(DSC2):c.627T>C (p.Phe209=)	rs754168300	0.00001
NM_024422.6(DSC2):c.2365GGA[1] (p.Gly790del)	rs377272752
NM_024422.6(DSC2):c.475-13A>G	rs751631188

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