List of variants reported as benign for Atypical hemolytic-uremic syndrome with B factor anomaly by Illumina Laboratory Services, Illumina

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Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_001710.6(CFB):c.450A>G (p.Arg150=)	rs1048709	0.85323
NM_001710.5(CFB):c.94C>T (p.Arg32Trp)	rs12614	0.17324
NM_001710.5(CFB):c.95G>A (p.Arg32Gln)	rs641153	0.11820
NM_001710.6(CFB):c.*23C>T	rs4151672	0.03305
NM_001710.6(CFB):c.504G>A (p.Pro168=)	rs4151669	0.03288
NM_001710.6(CFB):c.754G>A (p.Gly252Ser)	rs4151651	0.02344
NM_001710.6(CFB):c.672C>T (p.Tyr224=)	rs4151670	0.02070
NM_001710.6(CFB):c.1365C>T (p.Val455=)	rs2072634	0.01961
NM_001710.6(CFB):c.1693A>G (p.Lys565Glu)	rs4151659	0.01851
NM_001710.6(CFB):c.405C>T (p.Tyr135=)	rs4151650	0.01202
NM_001710.6(CFB):c.1697A>C (p.Glu566Ala)	rs45484591	0.00913
NM_001710.6(CFB):c.1137C>T (p.Arg379=)	rs45600936	0.00911
NM_001710.6(CFB):c.1953T>G (p.Asp651Glu)	rs4151660	0.00673
NM_001710.6(CFB):c.600C>T (p.Ser200=)	rs113197809	0.00527
NM_001710.6(CFB):c.1778+9G>A	rs188688680	0.00301
NM_001710.6(CFB):c.1143C>T (p.Arg381=)	rs150920440	0.00175
NM_001710.6(CFB):c.*47C>T	rs375895797	0.00052
NM_001710.6(CFB):c.2100C>T (p.Gly700=)	rs116928087	0.00017
NM_001710.6(CFB):c.1548G>A (p.Val516=)	rs553118090	0.00005
NM_001710.6(CFB):c.1956+10G>A	rs545348156	0.00001
NM_001710.6(CFB):c.1037-10C>G	rs201659953
NM_001710.6(CFB):c.1037-10C>T	rs201659953
NM_001710.6(CFB):c.1524C>T (p.His508=)	rs138207668

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