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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNKSR1
(P26fs +2 more)
Deletion
(frameshift variant)
not specified
+2 more
GBenign
CNKSR1
(R488C +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance