ClinVar Miner

Submissions for variant NM_000267.3(NF1):c.1070T>C (p.Leu357Pro) (rs137854563)

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
Center for Human Genetics, Inc,Center for Human Genetics, Inc RCV000000398 SCV000781892 pathogenic Neurofibromatosis, type 1 2016-11-01 criteria provided, single submitter clinical testing
OMIM RCV000000398 SCV000020542 pathogenic Neurofibromatosis, type 1 2000-03-01 no assertion criteria provided literature only
OMIM RCV000000399 SCV000020543 pathogenic Neurofibromatosis, familial spinal 2000-03-01 no assertion criteria provided literature only

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.