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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129993082, LOC129993083
+661 more
Copy number gain
See cases
GPathogenic
PITX2, LOC129992966
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign