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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC17A5
(V453fs)
Insertion
(frameshift variant)
Salla disease
+1 more
GConflicting classifications of pathogenicity
SLC17A5
(G265R +6 more)
Single nucleotide variant
(missense variant)
Sialic acid storage disease, severe infantile type
GLikely pathogenic