ClinVar Miner

Submissions for variant NM_000051.4(ATM):c.3402+16A>G

gnomAD frequency: 0.00002  dbSNP: rs763382531
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000581378 SCV000687470 likely benign Hereditary cancer-predisposing syndrome 2016-11-22 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000590240 SCV000694260 uncertain significance not provided 2016-03-18 criteria provided, single submitter clinical testing
GeneDx RCV000590240 SCV001945470 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Invitae RCV002060596 SCV002416534 likely benign Ataxia-telangiectasia syndrome 2024-01-24 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316756 SCV004016719 likely benign Familial cancer of breast 2023-07-07 criteria provided, single submitter clinical testing

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.