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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
H3-3A
(T46N)
Single nucleotide variant
(missense variant)
Bryant-Li-Bhoj neurodevelopmental syndrome 1
GUncertain significance
H3-3A
(M121I)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic