List of variants in gene SMAD3 reported as likely pathogenic by Genetics Department, University Hospital of Toulouse

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.334_335delinsCT (p.Ala112Leu)	rs1595941823
NM_005902.4(SMAD3):c.788C>T (p.Pro263Leu)	rs387906855
NM_005902.4(SMAD3):c.991G>T (p.Val331Phe)	rs1320208623

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