ClinVar Miner

List of variants in gene SMAD4 reported as likely benign by University of Washington Department of Laboratory Medicine,University of Washington

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_005359.5(SMAD4):c.-127-135A>C rs181270148
NM_005359.5(SMAD4):c.-127-3318A>G rs191217645
NM_005359.5(SMAD4):c.-127-4835G>A rs146792006
NM_005359.5(SMAD4):c.-127-4838G>A rs145288509
NM_005359.5(SMAD4):c.-128+1995A>G rs869312651
NM_005359.5(SMAD4):c.-128+263G>C rs149534722
NM_005359.5(SMAD4):c.-128+3139C>T rs75913646
NM_005359.5(SMAD4):c.-128+540A>G rs142196376
NM_005359.5(SMAD4):c.-128+759G>A rs9961921
NM_005359.5(SMAD4):c.1308+2398T>G rs79208698
NM_005359.5(SMAD4):c.1308+4116C>T rs869312653
NM_005359.5(SMAD4):c.1308+623C>T rs146176832
NM_005359.5(SMAD4):c.1448-113T>C rs145011178
NM_005359.5(SMAD4):c.250-589A>G rs869312650
NM_005359.5(SMAD4):c.424+165A>G rs182981059
NM_005359.5(SMAD4):c.454+291T>A rs182939830
NM_005359.5(SMAD4):c.455-1921T>G rs869312652
NM_005359.5(SMAD4):c.667+299T>C rs869312648
NM_005359.5(SMAD4):c.667+54T>C rs371193569
NM_005359.5(SMAD4):c.668-1111A>G rs140846022
NM_005359.5(SMAD4):c.787+15T>C rs374687785
NM_005359.5(SMAD4):c.904+298T>C rs869312649

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