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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT5B
(N106I +4 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 51
GPathogenic
KMT5B
(H110D +3 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual disability, autosomal dominant 51
GPathogenic