List of variants in gene CFHR4 reported as likely benign 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001201550.3(CFHR4):c.228T>C (p.Asp76=)	rs145744152	0.00846
NM_001201550.3(CFHR4):c.128A>T (p.Tyr43Phe)

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