List of variants in gene SMAD2 reported as likely pathogenic for hereditary disorder of connective tissue

Minimum submission review status:		Collection method:
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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_005901.6(SMAD2):c.1059T>G (p.Ser353Arg)
NM_005901.6(SMAD2):c.237-2A>G
NM_005901.6(SMAD2):c.507_508del (p.Arg169fs)
NM_005901.6(SMAD2):c.908C>G (p.Thr303Arg)	rs2144300077

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