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Items: 25

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMAD4
Single nucleotide variant
(5 prime UTR variant)
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome
+4 more
GUncertain significance
SMAD4
(T7M)
Single nucleotide variant
(missense variant)
not provided
+8 more
GConflicting classifications of pathogenicity
SMAD4
(M24V)
Single nucleotide variant
(missense variant)
Heritable Thoracic Aortic Disease
+7 more
GUncertain significance
SMAD4
(D52V)
Single nucleotide variant
(missense variant)
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome
+7 more
GUncertain significance
SMAD4
(I58V)
Single nucleotide variant
(missense variant)
Juvenile polyposis syndrome
+8 more
GUncertain significance
SMAD4
(I61V)
Single nucleotide variant
(missense variant)
not provided
+8 more
GUncertain significance
SMAD4
(I179V)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+7 more
GUncertain significance
SMAD4
(R189H)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+8 more
GConflicting classifications of pathogenicity
SMAD4
(Q224L)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+8 more
GConflicting classifications of pathogenicity
SMAD4
(A226V)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GConflicting classifications of pathogenicity
SMAD4
(G230R)
Single nucleotide variant
(missense variant)
Juvenile polyposis syndrome
+3 more
GUncertain significance
SMAD4
(Y276F)
Single nucleotide variant
(missense variant)
Juvenile polyposis syndrome
+6 more
GUncertain significance
SMAD4
(P303H)
Single nucleotide variant
(missense variant)
Juvenile polyposis syndrome
+6 more
GUncertain significance
SMAD4
(N306S)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+7 more
GUncertain significance
SMAD4
(R361H)
Single nucleotide variant
(missense variant)
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome
+7 more
GPathogenic/Likely pathogenic
SMAD4
(N369S)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GConflicting classifications of pathogenicity
SMAD4
Single nucleotide variant
(synonymous variant)
Carcinoma of pancreas
+5 more
GLikely benign
SMAD4
Single nucleotide variant
(intron variant)
Familial thoracic aortic aneurysm and aortic dissection
+8 more
GConflicting classifications of pathogenicity
SMAD4
(V407L)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+7 more
GConflicting classifications of pathogenicity
SMAD4
(M447L)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+5 more
GUncertain significance
SMAD4
(R496C)
Single nucleotide variant
(missense variant)
Myhre syndrome
+7 more
GConflicting classifications of pathogenicity
SMAD4
(I500V)
Single nucleotide variant
(missense variant)
Neurodevelopmental delay
+9 more
GPathogenic
SMAD4
(M543I)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GUncertain significance
SMAD4
(L551V)
Single nucleotide variant
(missense variant)
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome
+6 more
GUncertain significance
SMAD4
Single nucleotide variant
(3 prime UTR variant)
Juvenile polyposis syndrome
+4 more
GUncertain significance
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