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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WDFY3
(K2559R)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder
GUncertain significance
WDFY3
Single nucleotide variant
(splice donor variant)
Neurodevelopmental disorder
GUncertain significance