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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INPP5E
(A462V +1 more)
Single nucleotide variant
(missense variant)
INPP5E-related condition
+3 more
GUncertain significance
INPP5E
(R435Q +1 more)
Single nucleotide variant
(missense variant)
Retinal dystrophy
+3 more
GPathogenic/Likely pathogenic