List of variants in gene SMAD4 reported as likely benign by Counsyl

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_005359.6(SMAD4):c.880A>G (p.Met294Val)	rs7238500	0.00050
NM_005359.6(SMAD4):c.102A>G (p.Thr34=)	rs146104321	0.00032
NM_005359.6(SMAD4):c.904+14T>C	rs200973136	0.00017
NM_005359.6(SMAD4):c.21G>A (p.Thr7=)	rs142292491	0.00010
NM_005359.6(SMAD4):c.424+5G>A	rs200772603	0.00010
NM_005359.6(SMAD4):c.852A>G (p.Gln284=)	rs144378484	0.00008
NM_005359.6(SMAD4):c.606C>G (p.Ala202=)	rs780665234	0.00006
NM_005359.6(SMAD4):c.667+9T>C	rs776523203	0.00006
NM_005359.6(SMAD4):c.1653A>G (p.Leu551=)	rs199526820	0.00004
NM_005359.6(SMAD4):c.1140-11T>A	rs1224777335	0.00002
NM_005359.6(SMAD4):c.1422A>C (p.Ser474=)	rs786201261	0.00001
NM_005359.6(SMAD4):c.249+10A>C	rs752243771	0.00001
NM_005359.6(SMAD4):c.249+9T>C	rs770523387	0.00001
NM_005359.6(SMAD4):c.693C>T (p.Gly231=)	rs765597059	0.00001
NM_005359.6(SMAD4):c.1248A>G (p.Arg416=)	rs786202472
NM_005359.6(SMAD4):c.956-7C>T	rs778959035

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