List of variants in gene DSC2 reported as likely pathogenic for arrhythmogenic right ventricular dysplasia 11

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_024422.6(DSC2):c.943-1G>A	rs796756333	0.00002
NM_024422.6(DSC2):c.631-2A>G	rs397514042	0.00001
NC_000018.10:g.(?_31068005)_(31070860_?)del
NC_000018.9:g.(?_28673502)_(28673626_?)dup
NM_024422.6(DSC2):c.1264-1G>A	rs2144814453
NM_024422.6(DSC2):c.1520+1G>A
NM_024422.6(DSC2):c.154+2T>C	rs747424133
NM_024422.6(DSC2):c.1664-1G>C	rs776877367
NM_024422.6(DSC2):c.1888+1G>C	rs1986950096
NM_024422.6(DSC2):c.1888+2T>C
NM_024422.6(DSC2):c.1920dup (p.Pro641fs)	rs2144791672
NM_024422.6(DSC2):c.2125+1del	rs794728072
NM_024422.6(DSC2):c.2152del (p.Ala718fs)	rs760915248
NM_024422.6(DSC2):c.2250+1G>C	rs1986794200
NM_024422.6(DSC2):c.2250+2T>C	rs1064793731
NM_024422.6(DSC2):c.355-1G>A	rs2144843645
NM_024422.6(DSC2):c.474+1G>T	rs2144842978
NM_024422.6(DSC2):c.474+2T>A	rs1430478589
NM_024422.6(DSC2):c.749T>C (p.Phe250Ser)	rs746173561
NM_024422.6(DSC2):c.846C>G (p.Tyr282Ter)	rs397517406
NM_024422.6(DSC2):c.880del (p.Leu294fs)	rs1451144520

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