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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACUL1, PLPP4
+22 more
Copy number loss
Astigmatism
+4 more
GUncertain significance
ELP4, PAX6
(K387* +4 more)
Single nucleotide variant
(3 prime UTR variant +3 more)
Aniridia 1
+8 more
GConflicting classifications of pathogenicity