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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMAD3
(T57P)
Single nucleotide variant
(missense variant)
Loeys-Dietz syndrome
GUncertain significance
SMAD3
(Y88C +1 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+1 more
GUncertain significance
SMAD3
(V122M +2 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GPathogenic/Likely pathogenic
SMAD3
(P28fs +2 more)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
SMAD3
(G159S +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMAD3
(G245R +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
SMAD3
(R287W +3 more)
Single nucleotide variant
(missense variant)
Ehlers-Danlos syndrome
+3 more
GPathogenic/Likely pathogenic
SMAD3
(R287Q +3 more)
Single nucleotide variant
(missense variant)
Aneurysm-osteoarthritis syndrome
+3 more
GPathogenic/Likely pathogenic
SMAD3
(G291R +3 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
GUncertain significance
SMAD3
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
SMAD3
(R323H +3 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GConflicting classifications of pathogenicity
SMAD3
(V377I +3 more)
Single nucleotide variant
(missense variant)
Aneurysm-osteoarthritis syndrome
+1 more
GConflicting classifications of pathogenicity
SMAD3
(I396T +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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