List of variants reported as benign for Common variable immunodeficiency 1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

Download table as spreadsheet

HGVS	dbSNP
NM_012092.3(ICOS):c.*1024C>T	rs10932037
NM_012092.3(ICOS):c.*1095A>G	rs73991307
NM_012092.3(ICOS):c.*1249G>A	rs73991308
NM_012092.3(ICOS):c.*1262A>G	rs10932038
NM_012092.3(ICOS):c.*1407G>A	rs1559931
NM_012092.3(ICOS):c.*1773G>C	rs4675379
NM_012092.3(ICOS):c.*330G>A	rs10932035
NM_012092.3(ICOS):c.*33T>C	rs73058105
NM_012092.3(ICOS):c.*855T>C	rs73991306
NM_012092.3(ICOS):c.*859A>T	rs10932036
NM_012092.3(ICOS):c.*964T>C	rs4404254
NM_012092.3(ICOS):c.150A>G (p.Gln50=)	rs55972840
NM_012092.3(ICOS):c.40C>T (p.Arg14Cys)	rs77411896
NM_012092.3(ICOS):c.501+7G>A	rs57149344
NM_012092.3(ICOS):c.58+9T>G	rs140049646
NM_012092.3(ICOS):c.591G>A (p.Val197=)	rs55655222
NM_012092.4(ICOS):c.*2A>C	rs10183087
NM_012092.4(ICOS):c.375A>G (p.Gly125=)	rs768500706
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.