List of variants in gene CFHR3 reported as benign for anemia

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_021023.6(CFHR3):c.424C>T (p.Arg142Cys)	rs61737525	0.02034
NM_021023.6(CFHR3):c.720G>C (p.Gln240His)	rs149347641	0.01005

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