"Fulgent Genetics, Fulgent Genetics"[submitter] AND "GFI1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1170883	NM_005263.5(GFI1):c.925-40CT[21]	GFI1	Microsatellite (intron variant)	Neutropenia, severe congenital, 2, autosomal dominant +2 more	GBenign
Select item 402897	NM_005263.5(GFI1):c.925-40CT[19]	GFI1	Microsatellite (intron variant)	Nonimmune chronic idiopathic neutropenia of adults +2 more	GBenign/Likely benign
Select item 298185	NM_005263.5(GFI1):c.925-40CT[15]	GFI1	Microsatellite (intron variant)	Neutropenia, severe congenital, 2, autosomal dominant +3 more	GBenign/Likely benign
Select item 298188	NM_005263.5(GFI1):c.792C>T (p.Phe264=)	GFI1	Single nucleotide variant (synonymous variant)	Neutropenia, severe congenital, 2, autosomal dominant +3 more	GBenign/Likely benign
Select item 636791	NM_005263.5(GFI1):c.733T>C (p.Cys245Arg)	GFI1 (C245R)	Single nucleotide variant (missense variant)	Nonimmune chronic idiopathic neutropenia of adults +2 more	GUncertain significance
Select item 1517491	NM_005263.5(GFI1):c.233G>C (p.Ser78Thr)	GFI1 (S78T)	Single nucleotide variant (missense variant)	Neutropenia, severe congenital, 2, autosomal dominant +2 more	GConflicting classifications of pathogenicity

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