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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PIK3CA
Deletion
(inframe_deletion)
not provided
GLikely pathogenic
PIK3CA
Single nucleotide variant
(intron variant)
Cowden syndrome 5
+3 more
GBenign
PIK3CA
(K884R)
Single nucleotide variant
(missense variant)
not provided
+16 more
GUncertain significance
PIK3CA
Single nucleotide variant
(synonymous variant)
Cowden syndrome
+2 more
GConflicting classifications of pathogenicity
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