ClinVar Miner

List of variants in gene NTRK1 reported as uncertain significance for Hereditary insensitivity to pain with anhidrosis; Familial medullary thyroid carcinoma

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP
NM_001007792.1(NTRK1):c.1372C>A (p.Pro458Thr) rs764737760
NM_001007792.1(NTRK1):c.1997G>A (p.Arg666His) rs200022271
NM_001007792.1(NTRK1):c.2114C>T (p.Thr705Met) rs145081333

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.