ClinVar Miner

Submissions for variant NM_000138.5(FBN1):c.5672-15C>G

gnomAD frequency: 0.00006  dbSNP: rs776163620
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Total submissions: 12
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000292177 SCV000392288 uncertain significance Stiff skin syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000349467 SCV000392289 uncertain significance Familial thoracic aortic aneurysm and aortic dissection 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000383089 SCV000392290 uncertain significance Weill-Marchesani syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000291988 SCV000392291 uncertain significance MASS syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000344528 SCV000392292 uncertain significance Ectopia lentis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000405016 SCV000392293 uncertain significance Geleophysic dysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000304842 SCV000392294 uncertain significance Acromicric dysplasia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000343242 SCV000392295 uncertain significance Marfan syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV000840665 SCV000982593 likely benign not provided 2018-03-19 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.
Color Diagnostics, LLC DBA Color Health RCV000349467 SCV001354417 benign Familial thoracic aortic aneurysm and aortic dissection 2018-11-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003765836 SCV004594958 benign Marfan syndrome; Familial thoracic aortic aneurysm and aortic dissection 2023-12-18 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000343242 SCV004819862 benign Marfan syndrome 2023-11-30 criteria provided, single submitter clinical testing

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