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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STX11
(L58P)
Single nucleotide variant
(missense variant)
Familial hemophagocytic lymphohistiocytosis
+2 more
GPathogenic
STX11
(V124fs)
Indel
(frameshift variant)
not provided
GPathogenic