List of variants in gene SPI1 reported as likely pathogenic 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_003120.3(SPI1):c.573G>A (p.Trp191Ter)
NM_003120.3(SPI1):c.632A>C (p.His211Pro)	rs2095906547
NM_003120.3(SPI1):c.689G>C (p.Arg230Pro)
NM_003120.3(SPI1):c.722T>G (p.Val241Gly)	rs2095906404

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