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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2B
(S9fs)
Duplication
(frameshift variant +1 more)
Inborn genetic diseases
+2 more
GPathogenic
KMT2B
(A40fs)
Deletion
(frameshift variant)
Dystonia 28, childhood-onset
GPathogenic
KMT2B
(C1644F)
Single nucleotide variant
(missense variant)
Dystonia 28, childhood-onset
GLikely pathogenic
KMT2B
(T2539fs)
Deletion
(frameshift variant)
Dystonia 28, childhood-onset
GPathogenic
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