ClinVar Miner

Submissions for variant NM_001330195.2(NRXN3):c.758-160258G>A

gnomAD frequency: 0.01113  dbSNP: rs117696080
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
CeGaT Center for Human Genetics Tuebingen RCV003389828 SCV004130206 benign not provided 2022-12-01 criteria provided, single submitter clinical testing NRXN3: BS1, BS2
Michaelson Lab, University of Iowa RCV000722090 SCV000853276 uncertain significance Autism 2018-08-01 no assertion criteria provided research

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.