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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STAT3
(P715L +9 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+6 more
GPathogenic/Likely pathogenic
STAT3
(R382W +4 more)
Single nucleotide variant
(missense variant)
Hyper-IgE recurrent infection syndrome 1, autosomal dominant
+3 more
GPathogenic