ClinVar Miner

Submissions for variant NM_000037.4(ANK1):c.4538-52G>C

dbSNP: rs499295
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
Genome-Nilou Lab RCV001553992 SCV001775127 benign Hereditary spherocytosis type 1 2021-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001615310 SCV001837444 benign not provided 2021-06-18 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001615310 SCV005265337 benign not provided criteria provided, single submitter not provided

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.