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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CC2D2A
(E229del +1 more)
Microsatellite
(inframe_deletion)
Familial aplasia of the vermis
+5 more
GBenign/Likely benign
CC2D2A
(Q1096H +1 more)
Single nucleotide variant
(missense variant)
Ciliopathy
+3 more
GConflicting classifications of pathogenicity
CC2D2A
(E1259* +1 more)
Duplication
(nonsense)
Familial aplasia of the vermis
+5 more
GPathogenic
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