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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CERKL
(R461* +4 more)
Single nucleotide variant
(nonsense +1 more)
Retinitis pigmentosa 26
+3 more
GPathogenic/Likely pathogenic
CERKL
Microsatellite
(splice donor variant)
Retinitis pigmentosa 26
+1 more
GPathogenic/Likely pathogenic
CERKL
Deletion
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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