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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMAD4
(I40T)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
SMAD4
(H111L)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+2 more
GUncertain significance
SMAD4
(N151D)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
SMAD4
(P470S)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
SMAD4
(R496C)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GConflicting classifications of pathogenicity
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