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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXC1
(W152C)
Single nucleotide variant
(missense variant)
Axenfeld-Rieger syndrome type 3
GLikely pathogenic
FOXC1
(P219S)
Single nucleotide variant
(missense variant)
Axenfeld-Rieger syndrome type 3
GUncertain significance