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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
JAG1
(E1003fs)
Duplication
(frameshift variant)
Alagille syndrome due to a JAG1 point mutation
GLikely pathogenic
JAG1
(G386R)
Single nucleotide variant
(missense variant)
JAG1-related condition
+1 more
GPathogenic/Likely pathogenic
JAG1
(C187R)
Single nucleotide variant
(missense variant)
Alagille syndrome due to a JAG1 point mutation
GUncertain significance
JAG1
(R184C)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
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