List of variants in gene DSC2 reported as likely benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_024422.6(DSC2):c.1719C>T (p.Asn573=)	rs140167653	0.00590
NM_024422.6(DSC2):c.2616C>T (p.Cys872=)	rs61731920	0.00194
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.270G>A (p.Glu90=)	rs138643506	0.00056
NM_024422.6(DSC2):c.397G>A (p.Ala133Thr)	rs200218585	0.00004
NM_024422.6(DSC2):c.1350A>G (p.Arg450=)	rs144242114
NM_024422.6(DSC2):c.1371A>G (p.Thr457=)	rs1555638728

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