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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2D
(A5436fs)
Deletion
(frameshift variant)
Kabuki syndrome 1
GPathogenic
KMT2D
(S4907fs)
Deletion
(frameshift variant)
Kabuki syndrome 1
GPathogenic
KMT2D
(D4690Y)
Single nucleotide variant
(missense variant)
Kabuki syndrome 1
GUncertain significance
KMT2D
(K2063E)
Single nucleotide variant
(missense variant)
Kabuki syndrome 1
GUncertain significance
KMT2D
(S370fs)
Duplication
(frameshift variant)
Kabuki syndrome 1
GLikely pathogenic
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