ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.6472+14G>T

dbSNP: rs45503898
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244968 SCV000306112 benign not specified criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000726072 SCV000341738 uncertain significance not provided 2016-06-07 criteria provided, single submitter clinical testing
GeneDx RCV000726072 SCV001803408 likely benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000726072 SCV002407162 benign not provided 2024-01-29 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.