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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CERKL, LOC129935215
(W3*)
Single nucleotide variant
(nonsense +1 more)
Retinitis pigmentosa 26
+1 more
GPathogenic/Likely pathogenic
CERKL, LOC129935215
(W3fs)
Deletion
(frameshift variant +1 more)
Retinitis pigmentosa 26
GLikely pathogenic