List of variants reported as likely benign for Atypical hemolytic-uremic syndrome with C3 anomaly by Illumina Laboratory Services, Illumina

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000064.4(C3):c.2394C>T (p.Ser798=)	rs112178657	0.00228
NM_000064.4(C3):c.4827C>T (p.Ser1609=)	rs150537373	0.00035
NM_000064.4(C3):c.4824C>T (p.Ser1608=)	rs139457470	0.00034
NM_000064.4(C3):c.2157G>A (p.Ala719=)	rs143671993	0.00016
NM_000064.4(C3):c.681C>T (p.Tyr227=)	rs756694755	0.00012
NM_000064.4(C3):c.4535G>A (p.Arg1512His)	rs142868256	0.00009
NM_000064.4(C3):c.2207G>A (p.Arg736Gln)	rs578116271	0.00007
NM_000064.4(C3):c.1098A>G (p.Pro366=)	rs757883156	0.00006
NM_000064.4(C3):c.1119+10G>A	rs752328639	0.00006
NM_000064.4(C3):c.4471C>T (p.Arg1491Trp)	rs140928439	0.00006
NM_000064.4(C3):c.3953T>G (p.Leu1318Arg)	rs769873702	0.00005
NM_000064.4(C3):c.1164C>T (p.Pro388=)	rs769368306	0.00003
NM_000064.4(C3):c.1296G>A (p.Ser432=)	rs760150621	0.00001
NM_000064.4(C3):c.4850+12C>A	rs748416799	0.00001
NM_000064.4(C3):c.4941G>A (p.Gln1647=)	rs780251209	0.00001
NM_000064.4(C3):c.4645C>T (p.Leu1549=)	rs149202905
NM_000064.4(C3):c.4759C>T (p.Pro1587Ser)	rs746985605

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