ClinVar Miner

Submissions for variant NM_001130144.3(LTBP3):c.2033_2041delinsCTT (p.Asn678_Gly681delinsThrCys)

dbSNP: rs1856424871
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Washington Center for Mendelian Genomics, University of Washington RCV001291429 SCV001479931 confers sensitivity Heritable Thoracic Aortic Disease no assertion criteria provided research

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. The submitted information has not been verified. If you have questions about the information contained on this website, please see a health care professional.