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

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Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_000064.4(C3):c.-44C>T	rs773043245	0.00035
NM_000064.4(C3):c.1758G>A (p.Glu586=)	rs764201055	0.00007
NM_000064.4(C3):c.2907C>T (p.Asp969=)	rs144672500	0.00006
NM_000064.4(C3):c.4257G>A (p.Lys1419=)	rs768065757	0.00006
NM_000064.4(C3):c.1470C>T (p.Tyr490=)	rs762635358	0.00005
NM_000064.4(C3):c.1819A>G (p.Lys607Glu)	rs140637006	0.00005
NM_000064.4(C3):c.4095C>G (p.Val1365=)	rs527830114	0.00005
NM_000064.4(C3):c.4803C>T (p.His1601=)	rs762332809	0.00004
NM_000064.4(C3):c.3024G>A (p.Ser1008=)	rs779366181	0.00003
NM_000064.4(C3):c.3299T>C (p.Leu1100Pro)	rs750654763	0.00003
NM_000064.4(C3):c.4353C>G (p.Val1451=)	rs750821412	0.00003
NM_000064.4(C3):c.1303G>A (p.Glu435Lys)	rs774826179	0.00002
NM_000064.4(C3):c.3411C>T (p.Asn1137=)	rs753019751	0.00002
NM_000064.4(C3):c.3449C>G (p.Ser1150Trp)	rs1178318400	0.00002
NM_000064.4(C3):c.443G>A (p.Arg148Gln)	rs886054657	0.00002
NM_000064.4(C3):c.2441-6G>A	rs752216964	0.00001
NM_000064.4(C3):c.2646C>T (p.His882=)	rs377316231	0.00001
NM_000064.4(C3):c.267+9A>G	rs762058420	0.00001
NM_000064.4(C3):c.2793C>T (p.Val931=)	rs781226831	0.00001
NM_000064.4(C3):c.3970-15C>G	rs1233140401	0.00001
NM_000064.4(C3):c.4121-4C>T	rs747452882	0.00001
NM_000064.3(C3):c.-75A>C	rs1316357912
NM_000064.4(C3):c.1269+14C>A	rs886054655
NM_000064.4(C3):c.1686+10C>T	rs776885748
NM_000064.4(C3):c.1725T>C (p.Pro575=)	rs1967865144
NM_000064.4(C3):c.2390A>C (p.Asp797Ala)	rs1967690681
NM_000064.4(C3):c.2429C>T (p.Ser810Leu)	rs781280055
NM_000064.4(C3):c.2584G>T (p.Val862Leu)	rs1967565745
NM_000064.4(C3):c.2617T>C (p.Cys873Arg)	rs1967565177
NM_000064.4(C3):c.2670C>G (p.Pro890=)	rs137956083
NM_000064.4(C3):c.2700C>G (p.Ile900Met)	rs763155610
NM_000064.4(C3):c.2857G>A (p.Gly953Ser)	rs779124363
NM_000064.4(C3):c.2863+15G>T	rs759976981
NM_000064.4(C3):c.3407A>G (p.Asn1136Ser)	rs1918144043
NM_000064.4(C3):c.3586C>T (p.Leu1196=)	rs1918019867
NM_000064.4(C3):c.3793G>A (p.Gly1265Ser)	rs1918001974
NM_000064.4(C3):c.453C>T (p.Thr151=)	rs148870667
NM_000064.4(C3):c.819C>T (p.Phe273=)	rs886054656

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