List of variants in gene SMAD4 reported as uncertain significance 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_005359.6(SMAD4):c.565C>T (p.Arg189Cys)	rs140743238	0.00104
NM_005359.6(SMAD4):c.1573A>G (p.Ile525Val)	rs149755320	0.00071
NM_005359.6(SMAD4):c.521C>A (p.Thr174Asn)	rs138800446	0.00014
NM_005359.6(SMAD4):c.947A>G (p.Asn316Ser)	rs377119288	0.00005
NM_005359.6(SMAD4):c.20C>T (p.Thr7Met)	rs372316981	0.00003
NM_005359.6(SMAD4):c.575C>T (p.Thr192Ile)	rs587780792	0.00002
NM_005359.6(SMAD4):c.1046C>T (p.Thr349Ile)	rs564408927	0.00001
NM_005359.6(SMAD4):c.38A>G (p.Asn13Ser)	rs281875323	0.00001
NM_005359.6(SMAD4):c.449G>A (p.Ser150Asn)	rs750355699	0.00001
NM_005359.6(SMAD4):c.535A>G (p.Ile179Val)	rs542392980	0.00001
NM_005359.6(SMAD4):c.671A>T (p.Gln224Leu)	rs587780793	0.00001
NM_005359.6(SMAD4):c.743A>T (p.Gln248Leu)	rs751985298	0.00001
NM_005359.6(SMAD4):c.1647del (p.Gln549fs)	rs1555687615
NM_005359.6(SMAD4):c.172A>G (p.Ile58Val)	rs786204166
NM_005359.6(SMAD4):c.175A>G (p.Thr59Ala)	rs587781977
NM_005359.6(SMAD4):c.904T>C (p.Trp302Arg)	rs1555685979
NM_005359.6(SMAD4):c.910G>A (p.Val304Ile)	rs375185293

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