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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KMT2B
Single nucleotide variant
(intron variant)
Dystonia 28, childhood-onset
+1 more
GConflicting classifications of pathogenicity
KMT2B
(W1318L)
Single nucleotide variant
(missense variant)
Dystonia 28, childhood-onset
GUncertain significance