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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HDAC6
(G1078R +1 more)
Single nucleotide variant
(missense variant +1 more)
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
GUncertain significance
ARAF, CCDC120
+64 more
Copy number gain
not provided
GPathogenic