ClinVar Miner

List of variants studied for Immunodeficiency, common variable, 1 by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 52
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_012092.4(ICOS):c.*2A>C rs10183087 0.29378
NM_012092.4(ICOS):c.*964T>C rs4404254 0.29332
NM_012092.4(ICOS):c.*1407G>A rs1559931 0.29190
NM_012092.4(ICOS):c.*1773G>C rs4675379 0.14872
NM_012092.4(ICOS):c.*1262A>G rs10932038 0.08229
NM_012092.4(ICOS):c.*859A>T rs10932036 0.08225
NM_012092.4(ICOS):c.*330G>A rs10932035 0.08223
NM_012092.4(ICOS):c.*1024C>T rs10932037 0.08219
NM_012092.4(ICOS):c.*33T>C rs73058105 0.03775
NM_012092.4(ICOS):c.*1095A>G rs73991307 0.02660
NM_012092.4(ICOS):c.*855T>C rs73991306 0.02657
NM_012092.4(ICOS):c.150A>G (p.Gln50=) rs55972840 0.02252
NM_012092.4(ICOS):c.501+7G>A rs57149344 0.02252
NM_012092.4(ICOS):c.*1249G>A rs73991308 0.02203
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.*58T>G rs551768116 0.00008
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>G rs77882417
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
NM_012092.4(ICOS):c.501+6C>T rs4264550

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.