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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASAH1
(K152N +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
ASAH1
(Y153C +3 more)
Single nucleotide variant
(missense variant)
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome
+3 more
GPathogenic/Likely pathogenic