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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GPKOW
(T391I)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
GPKOW
(R339Q)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
GPKOW
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
GPKOW
(T51I)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
AWAT2, BCLAF3
+568 more
Copy number gain
not provided
GUncertain significance
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