ClinVar Miner

Submissions for variant NM_002506.3(NGF):c.321C>T (p.Val107=)

gnomAD frequency: 0.00004  dbSNP: rs202005277
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
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001802624 SCV002049108 likely benign Congenital sensory neuropathy with selective loss of small myelinated fibers 2020-12-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001802624 SCV004633553 likely benign Congenital sensory neuropathy with selective loss of small myelinated fibers 2024-04-24 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.