ClinVar Miner

Submissions for variant NM_005373.3(MPL):c.1566-7C>T

dbSNP: rs375344403
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
Invitae RCV001433551 SCV001636342 likely benign Congenital amegakaryocytic thrombocytopenia; Essential thrombocythemia 2024-01-30 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003405660 SCV004123655 uncertain significance not provided 2022-12-01 criteria provided, single submitter clinical testing MPL: PM2, BP4

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.