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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2A
(A89T)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
KMT2A
(R2214K +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
KMT2A
(T2733K +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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