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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCN6
(E102fs +1 more)
Deletion
(frameshift variant +1 more)
Progressive pseudorheumatoid dysplasia
+1 more
GPathogenic
CCN6
(W216C)
Single nucleotide variant
(missense variant +1 more)
Progressive pseudorheumatoid dysplasia
GUncertain significance