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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IRF7
(G247R +1 more)
Single nucleotide variant
(missense variant +1 more)
IRF7-related condition
+2 more
GConflicting classifications of pathogenicity
IRF7
(D217N +1 more)
Single nucleotide variant
(missense variant)
Immunodeficiency 39
+1 more
GLikely benign
IRF7
(R131Q +1 more)
Single nucleotide variant
(missense variant)
IRF7-related condition
+2 more
GConflicting classifications of pathogenicity
IRF7
Single nucleotide variant
(synonymous variant)
Immunodeficiency 39
GLikely benign
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