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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SKI
(P35A)
Single nucleotide variant
(missense variant)
Shprintzen-Goldberg syndrome
GLikely pathogenic
SKI
(P61L)
Single nucleotide variant
(missense variant)
Shprintzen-Goldberg syndrome
GUncertain significance
SKI
(I79M)
Single nucleotide variant
(missense variant)
Shprintzen-Goldberg syndrome
GLikely benign
SKI
(A472V)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GUncertain significance
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