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Links from OMIM

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STXBP2
Single nucleotide variant
(splice acceptor variant)
Familial hemophagocytic lymphohistiocytosis
+3 more
GPathogenic
STXBP2
(G541S +2 more)
Single nucleotide variant
(missense variant +1 more)
Familial hemophagocytic lymphohistiocytosis
+3 more
GPathogenic/Likely pathogenic
STXBP2
(P477L +2 more)
Single nucleotide variant
(missense variant +1 more)
Familial hemophagocytic lymphohistiocytosis 5
GPathogenic
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