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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXC1, LOC129995600
+1 more
(M1fs)
Deletion
(frameshift variant +1 more)
Axenfeld-Rieger syndrome type 3
GPathogenic
FOXC1
(A338fs)
Duplication
(frameshift variant)
Axenfeld-Rieger syndrome type 3
GPathogenic