ClinVar Miner

Submissions for variant NM_000133.4(F9):c.391+5G>A

dbSNP: rs2148358021
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University Hospital Muenster RCV001838829 SCV002098363 likely pathogenic Hereditary factor IX deficiency disease 2022-02-21 criteria provided, single submitter clinical testing ACMG categories: PM2,PP3,PP4,PP5

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.