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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLN5
(F139L)
Single nucleotide variant
(missense variant)
Neuronal ceroid lipofuscinosis 5
+2 more
GUncertain significance
CLN5
(R150*)
Single nucleotide variant
(nonsense)
Neuronal ceroid lipofuscinosis
+2 more
GPathogenic