List of variants in gene CFB reported as uncertain significance for atypical hemolytic-uremic syndrome with B factor anomaly

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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: 26

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HGVS	dbSNP	gnomAD frequency
NM_001710.6(CFB):c.724A>C (p.Ile242Leu)	rs144812066	0.00175
NM_001710.6(CFB):c.658+7T>C	rs541260302	0.00049
NM_001710.6(CFB):c.1407C>G (p.Ile469Met)	rs201798809	0.00019
NM_001710.6(CFB):c.1374G>A (p.Met458Ile)	rs200837114	0.00004
NM_001710.6(CFB):c.274A>T (p.Thr92Ser)	rs369638886	0.00004
NM_001710.6(CFB):c.*16A>T	rs749158582	0.00003
NM_001710.6(CFB):c.-3G>A	rs755016493	0.00003
NM_001710.6(CFB):c.1227A>G (p.Leu409=)	rs761050063	0.00003
NM_001710.6(CFB):c.1593T>C (p.Asp531=)	rs886061296	0.00003
NM_001710.6(CFB):c.321C>T (p.His107=)	rs767428982	0.00003
NM_001710.6(CFB):c.1290C>T (p.Val430=)	rs201619743	0.00002
NM_001710.6(CFB):c.118G>A (p.Glu40Lys)	rs1271096223	0.00001
NM_001710.6(CFB):c.1217G>A (p.Arg406Gln)	rs1057516209	0.00001
NM_001710.6(CFB):c.1762T>C (p.Tyr588His)	rs1364257553	0.00001
NM_001710.6(CFB):c.1861G>A (p.Glu621Lys)	rs573842877	0.00001
NM_001710.6(CFB):c.427C>T (p.Arg143Cys)	rs1242945827	0.00001
NM_001710.6(CFB):c.503C>T (p.Pro168Leu)	rs779024832	0.00001
NM_001710.6(CFB):c.917A>G (p.Lys306Arg)	rs374738591	0.00001
NM_001710.5(CFB):c.-199T>C	rs1771399314
NM_001710.6(CFB):c.1524C>A (p.His508Gln)	rs138207668
NM_001710.6(CFB):c.1803G>A (p.Glu601=)	rs377025675
NM_001710.6(CFB):c.1889C>T (p.Ala630Val)	rs886061297
NM_001710.6(CFB):c.2023G>A (p.Val675Met)
NM_001710.6(CFB):c.2069C>T (p.Ala690Val)	rs1403720810
NM_001710.6(CFB):c.334G>C (p.Gly112Arg)	rs950175817
NM_001710.6(CFB):c.656A>T (p.Gln219Leu)	rs886061295

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