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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GFI1
Microsatellite
(intron variant)
Severe congenital neutropenia
+2 more
GConflicting classifications of pathogenicity
GFI1
(A181T)
Single nucleotide variant
(missense variant)
Nonimmune chronic idiopathic neutropenia of adults
+2 more
GUncertain significance
GFI1
(D131N)
Single nucleotide variant
(missense variant)
Neutropenia, severe congenital, 2, autosomal dominant
+1 more
GUncertain significance
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