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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC17A5
Deletion
Sialic acid storage disease, severe infantile type
GPathogenic
SUOX
(C508fs)
Microsatellite
(frameshift variant)
SUOX-related condition
+1 more
GPathogenic/Likely pathogenic