ClinVar Miner

Submissions for variant NM_003640.5(ELP1):c.3977G>A (p.Trp1326Ter)

dbSNP: rs1554735724
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
Counsyl RCV000671681 SCV000796680 uncertain significance Familial dysautonomia 2017-12-21 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002477505 SCV002784830 uncertain significance Medulloblastoma; Familial dysautonomia 2022-03-16 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.