List of variants in gene CFB reported as benign for retinal disorder

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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_001710.6(CFB):c.*23C>T	rs4151672	0.03305
NM_001710.6(CFB):c.1693A>G (p.Lys565Glu)	rs4151659	0.01851
NM_001710.6(CFB):c.1697A>C (p.Glu566Ala)	rs45484591	0.00913
NM_001710.6(CFB):c.1953T>G (p.Asp651Glu)	rs4151660	0.00673

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