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

Minimum submission review status:		Collection method:
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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001110556.2(FLNA):c.6915C>T (p.Tyr2305=)	rs781910090	0.00002
NM_001110556.2(FLNA):c.7463C>A (p.Thr2488Asn)	rs909387820	0.00001
NM_001110556.2(FLNA):c.3103C>T (p.Pro1035Ser)
NM_001110556.2(FLNA):c.3497C>G (p.Ser1166Ter)
NM_001110556.2(FLNA):c.6793G>A (p.Glu2265Lys)	rs2148103563

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