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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2A
(Y1205* +1 more)
Single nucleotide variant
(nonsense)
Wiedemann-Steiner syndrome
GLikely pathogenic
KMT2A
(R1593fs +1 more)
Deletion
(frameshift variant)
Wiedemann-Steiner syndrome
GPathogenic
KMT2A
(E1984K +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
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