ClinVar Miner

Submissions for variant NM_012179.4(FBXO7):c.540A>G (p.Pro180=) (rs41311141)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000347464 SCV000437995 likely benign Parkinson Disease, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000546312 SCV000640391 benign Parkinson disease 15 2017-07-13 criteria provided, single submitter clinical testing
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000546312 SCV000744148 benign Parkinson disease 15 2015-09-21 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory,VU University Medical Center Amsterdam RCV000546312 SCV000745602 likely benign Parkinson disease 15 2016-07-21 no assertion criteria provided clinical testing

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.