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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WAS
(E278*)
Single nucleotide variant
(nonsense)
X-linked severe congenital neutropenia
GLikely pathogenic
WAS
(I294T)
Single nucleotide variant
(missense variant)
not provided
+5 more
GPathogenic/Likely pathogenic