ClinVar Miner

List of variants in gene CARMIL2 reported as benign for severe combined immunodeficiency due to CARMIL2 deficiency

Included ClinVar conditions (1):

Severe combined immunodeficiency due to CARMIL2 deficiency

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

Total variants: 2

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001013838.3(CARMIL2):c.1440-8T>C	rs9972635	0.15291
NM_001013838.3(CARMIL2):c.688-32C>T	rs59376497	0.11931

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.