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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEP290
(R1237fs)
Duplication
(frameshift variant)
Meckel syndrome, type 4
+4 more
GPathogenic/Likely pathogenic
CEP290
(M407fs)
Microsatellite
(frameshift variant)
Retinal dystrophy
+10 more
GPathogenic