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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PSAP
(K227del)
Deletion
(inframe_deletion)
Metachromatic leukodystrophy
+6 more
GPathogenic/Likely pathogenic
PSAP
(L118P)
Single nucleotide variant
(missense variant)
Combined PSAP deficiency
GUncertain significance