List of variants in gene SMAD4 reported as benign by Mayo Clinic Laboratories, Mayo Clinic

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005359.6(SMAD4):c.249+24A>G	rs77389132	0.00278
NM_005359.6(SMAD4):c.455-6A>G	rs181178864	0.00269
NM_005359.6(SMAD4):c.904+29A>T	rs543382977	0.00090
NM_005359.6(SMAD4):c.904+45del	rs386387676
NM_005359.6(SMAD4):c.904+45dup	rs386387676

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