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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNE
(V696M +5 more)
Single nucleotide variant
(missense variant)
GNE-related disorder
+3 more
GPathogenic/Likely pathogenic
GNE
(G471D +4 more)
Single nucleotide variant
(missense variant +1 more)
GNE myopathy
+1 more
GConflicting classifications of pathogenicity