List of variants in gene GFI1 reported as likely benign by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_005263.5(GFI1):c.168C>T (p.Ser56=)	rs143913803	0.00346
NM_005263.5(GFI1):c.792C>T (p.Phe264=)	rs114487177	0.00276
NM_005263.5(GFI1):c.319C>G (p.Pro107Ala)	rs149914857	0.00269
NM_005263.5(GFI1):c.63A>G (p.Pro21=)	rs142779589	0.00068
NM_005263.5(GFI1):c.1032C>T (p.Tyr344=)	rs139144506	0.00056
NM_005263.5(GFI1):c.-7G>A	rs184691209	0.00022
NM_005263.5(GFI1):c.252G>C (p.Ser84=)	rs140302204	0.00004
NM_005263.5(GFI1):c.597C>G (p.Leu199=)	rs1201094829
NM_005263.5(GFI1):c.925-7_925-6insTCTCTCTCTA	rs1553162639

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