ClinVar Miner

Submissions for variant NM_000132.4(F8):c.1097A>G (p.Asp366Gly)

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
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV005002120 SCV005627706 uncertain significance Hereditary factor VIII deficiency disease 2024-05-21 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV005244099 SCV005890851 uncertain significance not provided 2024-12-01 criteria provided, single submitter clinical testing F8: PM2

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.