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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STX11
(V34M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
STX11
(E206K)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
STX11
(Y255S)
Single nucleotide variant
(missense variant)
Familial hemophagocytic lymphohistiocytosis 4
+1 more
GUncertain significance
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