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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IFNGR1
(V118fs +2 more)
Deletion
(frameshift variant)
Immunodeficiency 27A
GPathogenic
IFNGR1
(W89R +2 more)
Single nucleotide variant
(missense variant)
Immunodeficiency 27A
GLikely pathogenic