List of variants reported as uncertain significance for Immunodeficiency, common variable, 1 by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 35

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HGVS	dbSNP	gnomAD frequency
NM_012092.4(ICOS):c.*995C>T	rs190590580	0.00677
NM_012092.4(ICOS):c.*1094C>T	rs144036725	0.00599
NM_012092.4(ICOS):c.*1300C>T	rs181937379	0.00360
NM_012092.4(ICOS):c.58+9T>G	rs140049646	0.00348
NM_012092.4(ICOS):c.451G>C (p.Val151Leu)	rs76778263	0.00226
NM_012092.4(ICOS):c.*1854G>A	rs140979765	0.00184
NM_012092.4(ICOS):c.*1137C>T	rs531066269	0.00123
NM_012092.4(ICOS):c.*1948G>T	rs777338223	0.00080
NM_012092.4(ICOS):c.*1416G>T	rs56259923	0.00071
NM_012092.4(ICOS):c.375A>G (p.Gly125=)	rs768500706	0.00064
NM_012092.4(ICOS):c.*1293T>C	rs528769953	0.00032
NM_012092.4(ICOS):c.*399G>A	rs760083763	0.00014
NM_012092.4(ICOS):c.*1004C>G	rs866710563	0.00013
NM_012092.4(ICOS):c.*1869A>C	rs931854904	0.00013
NM_012092.4(ICOS):c.591G>A (p.Val197=)	rs55655222	0.00012
NM_012092.4(ICOS):c.597A>G (p.Leu199=)	rs145698501	0.00011
NM_012092.4(ICOS):c.*939A>G	rs563893351	0.00006
NM_012092.4(ICOS):c.*77C>T	rs769887283	0.00005
NM_012092.4(ICOS):c.*512T>C	rs577478606	0.00004
NM_012092.4(ICOS):c.-24G>T	rs576726896	0.00003
NM_012092.4(ICOS):c.42C>A (p.Arg14=)	rs765158675	0.00003
NM_012092.4(ICOS):c.510A>G (p.Ser170=)	rs148435889	0.00003
NM_012092.4(ICOS):c.*594C>T	rs1391651175	0.00002
NM_012092.4(ICOS):c.*73T>C	rs756570847	0.00002
NM_012092.4(ICOS):c.*1269A>C	rs1430869619	0.00001
NM_012092.4(ICOS):c.*1457A>G	rs749858926	0.00001
NM_012092.4(ICOS):c.*931A>G	rs886055497	0.00001
NM_012092.4(ICOS):c.*1025A>T	rs77882417
NM_012092.4(ICOS):c.*1093C>T	rs886055499
NM_012092.4(ICOS):c.*1172G>A	rs1581609062
NM_012092.4(ICOS):c.*1901A>G	rs1690178448
NM_012092.4(ICOS):c.*474G>T	rs558652067
NM_012092.4(ICOS):c.*977T>G	rs886055498
NM_012092.4(ICOS):c.184C>T (p.Leu62Phe)	rs886055496
NM_012092.4(ICOS):c.495A>C (p.Thr165=)	rs565719501

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