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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STAT1
(T385M +9 more)
Single nucleotide variant
(missense variant)
Inherited Immunodeficiency Diseases
+17 more
GPathogenic
SCNN1A
(R476Q +2 more)
Single nucleotide variant
(missense variant)
not provided
+6 more
GConflicting classifications of pathogenicity