ClinVar Miner

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

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_001710.5(CFB):c.*23C>T rs4151672
NM_001710.5(CFB):c.*47C>T rs375895797
NM_001710.5(CFB):c.-186delG rs796979529
NM_001710.5(CFB):c.1037-10C>G rs201659953
NM_001710.5(CFB):c.1407C>G (p.Ile469Met) rs201798809
NM_001710.5(CFB):c.1693A>G (p.Lys565Glu) rs4151659
NM_001710.5(CFB):c.1697A>C (p.Glu566Ala) rs45484591
NM_001710.5(CFB):c.1778+9G>A rs188688680
NM_001710.5(CFB):c.2100C>T (p.Gly700=) rs116928087
NM_001710.5(CFB):c.604C>T (p.Arg202Trp) rs537478097
NM_001710.5(CFB):c.724A>C (p.Ile242Leu) rs144812066

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