List of variants in gene GFI1 studied for Severe congenital neutropenia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_005263.5(GFI1):c.925-40CT[13]	rs35896485
NM_005263.5(GFI1):c.925-40CT[15]	rs35896485
NM_005263.5(GFI1):c.925-40CT[16]	rs35896485
NM_005263.5(GFI1):c.925-40CT[17]	rs35896485
NM_005263.5(GFI1):c.925-40CT[20]	rs35896485
NM_005263.5(GFI1):c.925-40CT[22]	rs35896485
NM_005263.5(GFI1):c.925-40CT[23]	rs35896485
NM_005263.5(GFI1):c.925-40CT[25]	rs35896485
NM_005263.5(GFI1):c.925-7_925-6insTCTCTT	rs766365921

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