List of variants in gene ACTB 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001101.5(ACTB):c.1090G>A (p.Glu364Lys)	rs368352689
NM_001101.5(ACTB):c.458T>G (p.Met153Arg)
NM_001101.5(ACTB):c.583G>C (p.Glu195Gln)
NM_001101.5(ACTB):c.949delinsGAG (p.Ile317fs)	rs2128241225

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