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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UNC13D
Single nucleotide variant
(splice donor variant)
Autoinflammatory syndrome
+1 more
GPathogenic/Likely pathogenic
UNC13D
Single nucleotide variant
(intron variant)
Familial hemophagocytic lymphohistiocytosis
+2 more
GPathogenic/Likely pathogenic