ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.4637-110T>C

gnomAD frequency: 0.02262  dbSNP: rs74005837
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
GeneDx RCV001707865 SCV001935709 benign not provided 2019-05-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001707865 SCV005293913 benign not provided criteria provided, single submitter not provided
Leiden Open Variation Database RCV001194861 SCV001364697 likely benign not specified 2012-08-31 no assertion criteria provided curation Curator: Arleen D. Auerbach. Submitter to LOVD: Janine Bakker.

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.