List of variants in gene DSC2 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_024422.6(DSC2):c.1264-5C>T	rs183614856	0.00292
NM_024422.6(DSC2):c.1350A>G (p.Arg450=)	rs144242114
NM_024422.6(DSC2):c.2509-18T>C	rs1598569530

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