ClinVar Miner

List of variants reported as uncertain significance for Common variable immunodeficiency 1 by Illumina Clinical Services Laboratory,Illumina

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Minimum conflict level:
ClinVar version:
Total variants: 35
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HGVS dbSNP
NM_012092.3(ICOS):c.*1004C>G rs866710563
NM_012092.3(ICOS):c.*1093C>T rs886055499
NM_012092.3(ICOS):c.*1094C>T rs144036725
NM_012092.3(ICOS):c.*1293T>C rs528769953
NM_012092.3(ICOS):c.*1854G>A rs140979765
NM_012092.3(ICOS):c.*77C>T rs769887283
NM_012092.3(ICOS):c.*931A>G rs886055497
NM_012092.3(ICOS):c.*977T>G rs886055498
NM_012092.3(ICOS):c.*995C>T rs190590580
NM_012092.3(ICOS):c.184C>T (p.Leu62Phe) rs886055496
NM_012092.3(ICOS):c.451G>C (p.Val151Leu) rs76778263
NM_012092.3(ICOS):c.58+9T>G rs140049646
NM_012092.3(ICOS):c.591G>A (p.Val197=) rs55655222
NM_012092.3(ICOS):c.597A>G (p.Leu199=) rs145698501
NM_012092.4(ICOS):c.*1025A>T rs0
NM_012092.4(ICOS):c.*1137C>T rs0
NM_012092.4(ICOS):c.*1172G>A rs0
NM_012092.4(ICOS):c.*1269A>C rs0
NM_012092.4(ICOS):c.*1300C>T rs0
NM_012092.4(ICOS):c.*1416G>T rs0
NM_012092.4(ICOS):c.*1457A>G rs0
NM_012092.4(ICOS):c.*1869A>C rs0
NM_012092.4(ICOS):c.*1901A>G rs0
NM_012092.4(ICOS):c.*1948G>T rs0
NM_012092.4(ICOS):c.*399G>A rs0
NM_012092.4(ICOS):c.*474G>T rs0
NM_012092.4(ICOS):c.*512T>C rs0
NM_012092.4(ICOS):c.*594C>T rs0
NM_012092.4(ICOS):c.*73T>C rs0
NM_012092.4(ICOS):c.*939A>G rs0
NM_012092.4(ICOS):c.-24G>T rs0
NM_012092.4(ICOS):c.375A>G (p.Gly125=) rs768500706
NM_012092.4(ICOS):c.42C>A (p.Arg14=) rs0
NM_012092.4(ICOS):c.495A>C (p.Thr165=) rs0
NM_012092.4(ICOS):c.510A>G (p.Ser170=) rs0

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