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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNG2-DT, IFT27
+1 more
Single nucleotide variant
(splice donor variant)
not provided
GLikely pathogenic
IFT27
(G41R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance