List of variants in gene FLI1 reported as uncertain significance for hematologic disorder

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002017.5(FLI1):c.74C>T (p.Ala25Val)	rs200865469	0.00110
NM_002017.5(FLI1):c.203G>T (p.Arg68Leu)	rs201118331
NM_002017.5(FLI1):c.812G>A (p.Ser271Asn)	rs2135922425

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