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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTSD, PRADX
Single nucleotide variant
(synonymous variant)
Neuronal ceroid lipofuscinosis 10
+4 more
GBenign/Likely benign
CTSD, PRADX
(A58V)
Single nucleotide variant
(missense variant)
Neuronal ceroid lipofuscinosis 10
+4 more
GBenign/Likely benign