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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMAD3
Single nucleotide variant
(5 prime UTR variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GUncertain significance
SMAD3
Single nucleotide variant
(5 prime UTR variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GUncertain significance
SMAD3
(R80W +1 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
Aneurysm-osteoarthritis syndrome
+1 more
GUncertain significance
SMAD3
(M106T +2 more)
Single nucleotide variant
(missense variant +1 more)
Familial thoracic aortic aneurysm and aortic dissection
+2 more
GUncertain significance
SMAD3
(A112T +2 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+2 more
GUncertain significance
SMAD3
(T132A +2 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+2 more
GUncertain significance
SMAD3
Single nucleotide variant
(intron variant)
Connective tissue disorder
+3 more
GPathogenic/Likely pathogenic
SMAD3
(F106L +2 more)
Single nucleotide variant
(missense variant)
Aneurysm-osteoarthritis syndrome
+2 more
GUncertain significance
SMAD3
(A215T +3 more)
Single nucleotide variant
(missense variant)
Aneurysm-osteoarthritis syndrome
+1 more
GUncertain significance
SMAD3
(V303D +3 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
SMAD3
(A312T +3 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+2 more
GUncertain significance
SMAD3
(R128C +3 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+2 more
GUncertain significance
SMAD3
(N357S +3 more)
Single nucleotide variant
(missense variant)
Aneurysm-osteoarthritis syndrome
+2 more
GConflicting classifications of pathogenicity
SMAD3
(R420C +3 more)
Single nucleotide variant
(missense variant)
Aneurysm-osteoarthritis syndrome
+3 more
GUncertain significance
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