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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXO11
Single nucleotide variant
(intron variant)
Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities
GUncertain significance
FBXO11
(A276G +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities
GUncertain significance
FBXO11
Single nucleotide variant
(intron variant)
not provided
+1 more
GUncertain significance
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