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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFT140
(R871C)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa
+3 more
GConflicting classifications of pathogenicity
IFT140
Single nucleotide variant
(splice donor variant)
Autosomal dominant polycystic kidney disease
+6 more
GPathogenic