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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KLHL15
(E469G)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 103
GUncertain significance
KLHL15
(R274C)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 103
GUncertain significance
KLHL15
(K237M)
Single nucleotide variant
(missense variant)
Intellectual disability, X-linked 103
GUncertain significance
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