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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TGFB2
(R34H)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
TGFB2
(V67M)
Single nucleotide variant
(missense variant +1 more)
Familial thoracic aortic aneurysm and aortic dissection
+4 more
GUncertain significance