ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.75G>A (p.Leu25=) (rs200350612)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000756172 SCV000883898 benign not provided 2017-09-06 criteria provided, single submitter clinical testing
Ambry Genetics RCV000573433 SCV000673435 likely benign Hereditary cancer-predisposing syndrome 2015-06-09 criteria provided, single submitter clinical testing
Invitae RCV000474706 SCV000560340 benign Multiple fibrofolliculomas 2017-10-30 criteria provided, single submitter 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.