ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.863_866dup (p.Ser290fs) (rs1348367722)

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
Counsyl RCV000671112 SCV000796057 likely pathogenic Fanconi anemia, complementation group A 2017-11-28 criteria provided, single submitter clinical testing
Gharavi Laboratory,Columbia University RCV000722326 SCV000853457 uncertain significance not provided 2018-09-16 no assertion criteria provided research

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.