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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130067355, RAC2
Single nucleotide variant
(intron variant)
Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
+4 more
GBenign
LOC130067355, RAC2
Single nucleotide variant
(intron variant)
Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
+4 more
GBenign
RAC2
Duplication
(intron variant)
Neutrophil immunodeficiency syndrome
+4 more
GBenign
RAC2
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GBenign
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