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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NOTCH1
(R2327W)
Single nucleotide variant
(missense variant)
Aortic valve disease 1
+2 more
GConflicting classifications of pathogenicity
NOTCH1
(Q1810H)
Single nucleotide variant
(missense variant)
Aortic valve disease 1
GUncertain significance
NOTCH1
(V1739M)
Single nucleotide variant
(missense variant)
not provided
+7 more
GConflicting classifications of pathogenicity
NOTCH1
(G187R)
Single nucleotide variant
(missense variant)
Aortic valve disease 1
GUncertain significance
NOTCH1
(R112H)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+3 more
GUncertain significance
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