List of variants in gene combination DSC2, DSCAS reported as benign for cardiovascular disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_024422.6(DSC2):c.32A>G (p.Asn11Ser)	rs868333	0.08191
NM_024422.6(DSC2):c.34G>A (p.Gly12Arg)	rs568391206	0.00093

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