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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP1B1
(R368H)
Single nucleotide variant
(missense variant)
Congenital glaucoma
+7 more
GConflicting classifications of pathogenicity
SPEG
(G1587R)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance