ClinVar Miner

Submissions for variant NM_052867.4(NALCN):c.3843G>A (p.Thr1281=)

gnomAD frequency: 0.00057  dbSNP: rs151200877
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000995073 SCV001149068 uncertain significance not provided 2016-06-01 criteria provided, single submitter clinical testing
GeneDx RCV000995073 SCV001816241 likely benign not provided 2021-03-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000995073 SCV003284232 benign not provided 2025-02-02 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.