ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.1518G>A (p.Leu506=)

gnomAD frequency: 0.00004  dbSNP: rs759226270
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001469775 SCV001673863 likely benign Multiple gastrointestinal atresias 2024-01-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003884818 SCV004700091 likely benign not provided 2024-02-01 criteria provided, single submitter clinical testing TTC7A: BP4, BP7

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.