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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP290
(K1575*)
Single nucleotide variant
(nonsense)
Blindness
+13 more
GPathogenic
CEP290
(Q981*)
Single nucleotide variant
(nonsense)
Bardet-Biedl syndrome 14
+5 more
GPathogenic/Likely pathogenic