List of variants in gene DSC2 reported as uncertain significance by Stanford Center for Inherited Cardiovascular Disease, Stanford University

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: 11

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HGVS	dbSNP	gnomAD frequency
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.2587G>A (p.Gly863Arg)	rs147109895	0.00023
NM_024422.6(DSC2):c.2251-5T>G	rs374262463	0.00009
NM_024422.6(DSC2):c.82G>T (p.Ala28Ser)	rs139979318	0.00009
NM_024422.6(DSC2):c.408A>G (p.Arg136=)	rs561653481	0.00004
NM_024422.6(DSC2):c.321G>T (p.Lys107Asn)	rs140856220	0.00003
NM_024422.6(DSC2):c.1103C>T (p.Thr368Ile)	rs538663626	0.00001
NM_024422.6(DSC2):c.325A>C (p.Ile109Leu)	rs1256252633	0.00001
NM_024422.6(DSC2):c.1352C>T (p.Ser451Leu)	rs794728068
NM_024422.6(DSC2):c.2263G>A (p.Gly755Ser)	rs727502979

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