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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNE
(V696M +5 more)
Single nucleotide variant
(missense variant)
GNE-related condition
+3 more
GConflicting classifications of pathogenicity
GNE
(E134fs +2 more)
Duplication
(frameshift variant)
GNE myopathy
+1 more
GPathogenic
GNE
(E33* +1 more)
Single nucleotide variant
(nonsense +1 more)
not provided
+2 more
GPathogenic/Likely pathogenic
GNE myopathy
GPathogenic
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