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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TESK2
(R372C +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
AKR1A1, CCDC163
+22 more
Copy number gain
See cases
GUncertain significance
AKR1A1, CCDC17
+5 more
Copy number gain
See cases
GUncertain significance
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