ClinVar Miner

Variants in gene LTBP4 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 7
Download table as spreadsheet
NM_003573.2(LTBP4):c.1328G>A (p.Gly443Asp) rs114749335
NM_003573.2(LTBP4):c.1531A>G (p.Met511Val) rs116005784
NM_003573.2(LTBP4):c.1581G>T (p.Arg527=) rs117273116
NM_003573.2(LTBP4):c.2389+9A>G rs73544980
NM_003573.2(LTBP4):c.2526G>A (p.Val842=) rs371083223
NM_003573.2(LTBP4):c.3428G>A (p.Arg1143His) rs199887429
NM_003573.2(LTBP4):c.79C>T (p.Leu27=) rs370696272

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.