List of variants in gene VCL reported as uncertain significance for Dilated Cardiomyopathy, Dominant

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_014000.3(VCL):c.1849_1850insC	rs200756813	0.16729
NM_014000.3(VCL):c.*1282C>T	rs529687198	0.00054
NM_014000.3(VCL):c.*145del	rs756151016
NM_014000.3(VCL):c.1665_1669dup	rs886047227
NM_014000.3(VCL):c.*1705AAGA[3]	rs1554820063
NM_014000.3(VCL):c.1841_1842insA	rs886047231
NM_014000.3(VCL):c.1841_1842insAA	rs886047231
NM_014000.3(VCL):c.1860_1862dup	rs3037361
NM_014000.3(VCL):c.1861_1862dup	rs3037361
NM_014000.3(VCL):c.*353CT[1]	rs144115212
NM_014000.3(VCL):c.*709del	rs886047223

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