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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2D
(Q4223*)
Single nucleotide variant
(nonsense)
not provided
+3 more
GPathogenic
KMT2D
(R3582W)
Single nucleotide variant
(missense variant)
Kabuki syndrome
+3 more
GPathogenic/Likely pathogenic