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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GATAD2B
(Q482H)
Single nucleotide variant
(missense variant)
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
GLikely pathogenic
GATAD2B
(L256F)
Single nucleotide variant
(missense variant)
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
GUncertain significance
GATAD2B
Duplication
(splice donor variant)
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome
GUncertain significance
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