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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLN5, LOC130009913
(W26R)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
CLN5
(N193K)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
+4 more
GConflicting classifications of pathogenicity