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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATF1, DIP2B
+14 more
Copy number gain
See cases
GUncertain significance
SLC11A2
(R102H +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance