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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2D
(R5179H)
Single nucleotide variant
(missense variant)
Kabuki syndrome
+2 more
GPathogenic/Likely pathogenic
KMT2D
(W4730*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
KMT2D
(G398fs)
Deletion
(frameshift variant)
Kabuki syndrome 1
GPathogenic
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