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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IRF7
(Q421* +2 more)
Single nucleotide variant
(nonsense)
Immunodeficiency 39
GPathogenic
IRF7
(F410V +2 more)
Single nucleotide variant
(missense variant)
Immunodeficiency 39
GUncertain significance