ClinVar Miner

Submissions for variant NM_182961.4(SYNE1):c.18363C>T (p.Ala6121=)

gnomAD frequency: 0.00003  dbSNP: rs758953542
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 RCV001469738 SCV001673825 likely benign Autosomal recessive ataxia, Beauce type; Emery-Dreifuss muscular dystrophy 4, autosomal dominant 2022-09-07 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003434257 SCV004160536 likely benign not provided 2022-07-01 criteria provided, single submitter clinical testing SYNE1: 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.