"Genome Diagnostics Laboratory, University Medical Center Utrecht"[sub - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 470694	NM_005263.5(GFI1):c.1198C>T (p.Leu400Phe)	GFI1, LOC129930930 (L400F)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 1170883	NM_005263.5(GFI1):c.925-40CT[21]	GFI1	Microsatellite (intron variant)	not provided +3 more	GBenign
Select item 402897	NM_005263.5(GFI1):c.925-40CT[19]	GFI1	Microsatellite (intron variant)	Nonimmune chronic idiopathic neutropenia of adults +3 more	GBenign/Likely benign
Select item 298185	NM_005263.5(GFI1):c.925-40CT[15]	GFI1	Microsatellite (intron variant)	Severe congenital neutropenia +3 more	GBenign/Likely benign
Select item 298188	NM_005263.5(GFI1):c.792C>T (p.Phe264=)	GFI1	Single nucleotide variant (synonymous variant)	Nonimmune chronic idiopathic neutropenia of adults +3 more	GBenign/Likely benign
Select item 259703	NM_005263.5(GFI1):c.319C>G (p.Pro107Ala)	GFI1 (P107A)	Single nucleotide variant (missense variant)	not provided +2 more	GLikely benign
Select item 259699	NM_005263.5(GFI1):c.107G>A (p.Ser36Asn)	GFI1 (S36N)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign

ClinVar