List of variants in gene CD79A reported as 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
NC_000019.10:g.41878996_41879009del
NM_001783.4(CD79A):c.198G>A (p.Trp66Ter)	rs1568801716
NM_001783.4(CD79A):c.379+1G>A	rs1555843601
NM_001783.4(CD79A):c.380-2A>G	rs1600631593

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