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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CPLANE1
(R3020* +1 more)
Single nucleotide variant
(nonsense)
Joubert syndrome and related disorders
+5 more
GPathogenic/Likely pathogenic
CPLANE1
(Q855*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic