ClinVar Miner

Submissions for variant NM_000138.5(FBN1):c.6699C>T (p.Pro2233=)

gnomAD frequency: 0.00005  dbSNP: rs372386014
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV001526111 SCV000738831 likely benign Familial thoracic aortic aneurysm and aortic dissection 2016-08-11 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
Labcorp Genetics (formerly Invitae), Labcorp RCV001475094 SCV001679280 likely benign Marfan syndrome; Familial thoracic aortic aneurysm and aortic dissection 2024-01-18 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001526111 SCV001736396 likely benign Familial thoracic aortic aneurysm and aortic dissection 2020-12-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004002720 SCV004822435 likely benign Marfan syndrome 2024-02-05 criteria provided, single submitter clinical testing

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