List of variants in gene combination GFI1, LOC129930930 reported as likely benign for Neutropenia, severe congenital, 2, autosomal dominant

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_005263.5(GFI1):c.1091-5C>T	rs1385981170	0.00006
NM_005263.5(GFI1):c.1208A>G (p.Lys403Arg)	rs28936382	0.00004
NM_005263.5(GFI1):c.1119C>T (p.Cys373=)	rs780643435	0.00003
NM_005263.5(GFI1):c.1091-16C>G
NM_005263.5(GFI1):c.1091-19C>T
NM_005263.5(GFI1):c.1098G>A (p.Lys366=)
NM_005263.5(GFI1):c.1194C>T (p.Cys398=)	rs1348982767
NM_005263.5(GFI1):c.1209G>A (p.Lys403=)

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