List of variants in gene SMAD3 reported as likely pathogenic by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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_005902.4(SMAD3):c.1229_1244del (p.Val410fs)	rs1555414495
NM_005902.4(SMAD3):c.648del (p.His216fs)	rs1555412629
NM_005902.4(SMAD3):c.747del (p.His249fs)

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