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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KDM5B
(L1325V +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KDM5B
(T152S +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 65
GUncertain significance