List of variants in gene SMAD4 reported as benign by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005359.6(SMAD4):c.956-31G>A	rs11875522	0.04946
NM_005359.6(SMAD4):c.455-43A>T	rs149541014	0.00759
NM_005359.6(SMAD4):c.1308+33_1308+34del	rs201683280	0.00695
NM_005359.6(SMAD4):c.*11C>T	rs11663402	0.00538
NM_005359.6(SMAD4):c.249+24A>G	rs77389132	0.00278
NM_005359.6(SMAD4):c.904+43_904+45dup	rs386387676

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