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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRRAP
(L1177H)
Single nucleotide variant
(missense variant)
Developmental delay with or without dysmorphic facies and autism
GUncertain significance
TRRAP
(P3582S +2 more)
Single nucleotide variant
(missense variant)
Developmental delay with or without dysmorphic facies and autism
GUncertain significance