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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STX11
(E36Q)
Single nucleotide variant
(missense variant)
Familial hemophagocytic lymphohistiocytosis 4
GUncertain significance
STX11
(R49Q)
Single nucleotide variant
(missense variant)
Familial hemophagocytic lymphohistiocytosis 4
+3 more
GBenign/Likely benign
STX11
(M76I)
Single nucleotide variant
(missense variant)
Familial hemophagocytic lymphohistiocytosis 4
+1 more
GUncertain significance
STX11
(V197M)
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome
+2 more
GConflicting classifications of pathogenicity
STX11
(V267M)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
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