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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFT74
(I55L)
Single nucleotide variant
(missense variant)
IFT74-related condition
+3 more
GConflicting classifications of pathogenicity
IFT74
(V579M)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign/Likely benign