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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTSD, LOC130005119
(P3L)
Single nucleotide variant
(missense variant)
Neuronal ceroid lipofuscinosis
+3 more
GUncertain significance
CTSD, LOC130005119
Microsatellite
(inframe_insertion)
not provided
GUncertain significance