List of variants in gene CFB 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001710.6(CFB):c.600C>T (p.Ser200=)	rs113197809	0.00527
NM_001710.6(CFB):c.724A>C (p.Ile242Leu)	rs144812066	0.00175
NM_001710.6(CFB):c.1407C>G (p.Ile469Met)	rs201798809	0.00019
NM_001710.6(CFB):c.2100C>T (p.Gly700=)	rs116928087	0.00017
NM_001710.6(CFB):c.291G>A (p.Glu97=)	rs138236643	0.00014
NM_001710.6(CFB):c.1838C>T (p.Thr613Ile)	rs201754399	0.00007
NM_001710.6(CFB):c.784G>A (p.Val262Ile)	rs200645483	0.00007
NM_001710.6(CFB):c.1778+8C>T	rs148298609	0.00005
NM_001710.6(CFB):c.604C>T (p.Arg202Trp)	rs537478097	0.00004
NM_001710.6(CFB):c.720G>A (p.Glu240=)	rs753831049	0.00002
NM_001710.5(CFB):c.-186delG	rs796979529
NM_001710.6(CFB):c.1942A>T (p.Lys648Ter)	rs2151787951

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