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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLN8
(P171R)
Single nucleotide variant
(missense variant)
Neuronal ceroid lipofuscinosis 8
+1 more
GUncertain significance
CLN8
(M200fs)
Duplication
(frameshift variant)
Neuronal ceroid lipofuscinosis 8
+1 more
GPathogenic/Likely pathogenic
CLN8
(N264K)
Single nucleotide variant
(missense variant)
Neuronal ceroid lipofuscinosis 8
+1 more
GConflicting classifications of pathogenicity
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