ClinVar Miner

Variants in gene LTBP4 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 22
Download table as spreadsheet
NM_001042545.2(LTBP4):c.135C>T (p.Cys45=) rs185400394
NM_003573.2(LTBP4):c.1328G>A (p.Gly443Asp) rs114749335
NM_003573.2(LTBP4):c.1390T>A (p.Ser464Thr) rs34545902
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.1792C>G (p.Arg598Gly) rs33937741
NM_003573.2(LTBP4):c.1924C>G (p.Pro642Ala) rs34299942
NM_003573.2(LTBP4):c.2143G>A (p.Asp715Asn) rs34093919
NM_003573.2(LTBP4):c.2144-11C>A rs41470347
NM_003573.2(LTBP4):c.2265C>T (p.Cys755=) rs141810975
NM_003573.2(LTBP4):c.2328C>T (p.Pro776=) rs201588216
NM_003573.2(LTBP4):c.2389+9A>G rs73544980
NM_003573.2(LTBP4):c.2526G>A (p.Val842=) rs371083223
NM_003573.2(LTBP4):c.2541G>A (p.Glu847=) rs191216887
NM_003573.2(LTBP4):c.2655C>T (p.Asp885=) rs2077407
NM_003573.2(LTBP4):c.3219C>T (p.Val1073=) rs78745792
NM_003573.2(LTBP4):c.3349G>A (p.Val1117Ile) rs369582949
NM_003573.2(LTBP4):c.4298G>A (p.Arg1433His)
NM_003573.2(LTBP4):c.4388A>T (p.Tyr1463Phe) rs35809725
NM_003573.2(LTBP4):c.79C>T (p.Leu27=) rs370696272
NM_003573.2(LTBP4):c.948G>A (p.Gly316=) rs146234365
NM_003573.2(LTBP4):c.981C>T (p.Gly327=) rs374427407

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.