ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.872-4G>A (rs752727873)

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 RCV000536612 SCV000632898 likely benign Multiple fibrofolliculomas 2020-03-10 criteria provided, single submitter clinical testing
Ambry Genetics RCV001018238 SCV001179448 likely benign Hereditary cancer-predisposing syndrome 2019-10-16 criteria provided, single submitter clinical testing In silico models in agreement (benign);Intronic alteration with no splicing impact by rt-pcr analysis or other splicing assay

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.