ClinVar Miner

List of variants in gene CFB reported as likely benign for anemia (disease)

Included ClinVar conditions (281):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_001710.5(CFB):c.-186del rs796979529
NM_001710.5(CFB):c.1407C>G (p.Ile469Met) rs201798809
NM_001710.5(CFB):c.291G>A (p.Glu97=) rs138236643
NM_001710.5(CFB):c.604C>T (p.Arg202Trp) rs537478097
NM_001710.5(CFB):c.720G>A (p.Glu240=) rs753831049
NM_001710.5(CFB):c.724A>C (p.Ile242Leu) rs144812066
NM_001710.6(CFB):c.1838C>T (p.Thr613Ile)
NM_001710.6(CFB):c.784G>A (p.Val262Ile)

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