ClinVar Miner

List of variants in gene CFB studied for Atypical hemolytic uremic syndrome

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Total variants: 22
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NM_001710.5(CFB):c.*16A>T rs749158582
NM_001710.5(CFB):c.*23C>T rs4151672
NM_001710.5(CFB):c.*47C>T rs375895797
NM_001710.5(CFB):c.-186del rs796979529
NM_001710.5(CFB):c.-3G>A rs755016493
NM_001710.5(CFB):c.1037-10C>G rs201659953
NM_001710.5(CFB):c.1037-10C>T rs201659953
NM_001710.5(CFB):c.1227A>G (p.Leu409=) rs761050063
NM_001710.5(CFB):c.1407C>G (p.Ile469Met) rs201798809
NM_001710.5(CFB):c.1524C>A (p.His508Gln) rs138207668
NM_001710.5(CFB):c.1593T>C (p.Asp531=) rs886061296
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.1889C>T (p.Ala630Val) rs886061297
NM_001710.5(CFB):c.2100C>T (p.Gly700=) rs116928087
NM_001710.5(CFB):c.291G>A (p.Glu97=) rs138236643
NM_001710.5(CFB):c.321C>T (p.His107=) rs767428982
NM_001710.5(CFB):c.604C>T (p.Arg202Trp) rs537478097
NM_001710.5(CFB):c.656A>T (p.Gln219Leu) rs886061295
NM_001710.5(CFB):c.720G>A (p.Glu240=) rs753831049
NM_001710.5(CFB):c.724A>C (p.Ile242Leu) rs144812066

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