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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP290
(K1930*)
Single nucleotide variant
(nonsense)
Retinal dystrophy
+5 more
GPathogenic
CEP290
(Q1591*)
Single nucleotide variant
(nonsense)
Bardet-Biedl syndrome 14
+3 more
GPathogenic
CEP290
(R1465*)
Single nucleotide variant
(nonsense)
Bardet-Biedl syndrome 14
+9 more
GPathogenic
CEP290
(I556fs)
Deletion
(frameshift variant)
not provided
+10 more
GPathogenic
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