ClinVar Miner

Submissions for variant NM_002529.3(NTRK1):c.2202G>A (p.Thr734=) (rs55668752)

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 RCV000372018 SCV000349067 likely benign Hereditary insensitivity to pain with anhidrosis 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV000439601 SCV000530852 benign not specified 2016-09-20 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000755591 SCV000604571 benign not provided 2017-06-14 criteria provided, single submitter clinical testing
Invitae RCV000755591 SCV000626959 benign not provided 2019-03-05 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.