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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASB12
(R278W)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
ASB12
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ASB12
(A130P)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
AWAT2, BCLAF3
+568 more
Copy number gain
not provided
GUncertain significance
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