List of variants reported as benign for Combined immunodeficiency due to CD3gamma deficiency by Labcorp Genetics (formerly Invitae), Labcorp

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000073.3(CD3G):c.390T>C (p.Ala130=)	rs3753059	0.16289
NM_000073.3(CD3G):c.391G>T (p.Val131Phe)	rs3753058	0.16277
NM_000073.3(CD3G):c.64G>A (p.Ala22Thr)	rs139781104	0.00294
NM_000073.3(CD3G):c.79+10A>G	rs115851096	0.00266
NM_000073.3(CD3G):c.439+11G>A	rs187746068	0.00149
NM_000073.3(CD3G):c.496C>A (p.Arg166=)	rs201529449	0.00022
NM_000073.3(CD3G):c.390_391delinsCT (p.Val131Phe)	rs71469175
NM_000073.3(CD3G):c.440-7del	rs747939880

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.