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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCND2
(V284E)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely pathogenic
PIK3R2
(E274A)
Single nucleotide variant
(missense variant +1 more)
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1
GUncertain significance
PIK3R2
(G373R)
Single nucleotide variant
(missense variant +1 more)
Overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes
GPathogenic
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