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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CERKL
Deletion
(inframe_indel +2 more)
Retinitis pigmentosa 26
GUncertain significance
CERKL
(E18fs)
Deletion
(frameshift variant +1 more)
Retinitis pigmentosa 26
GLikely pathogenic