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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTEN
Single nucleotide variant
(synonymous variant +1 more)
PTEN hamartoma tumor syndrome
GLikely benign
PTEN
(D393G +2 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
GUncertain significance