ClinVar Miner

Submissions for variant NM_000138.5(FBN1):c.5842A>G (p.Ile1948Val)

gnomAD frequency: 0.00004  dbSNP: rs766850261
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001035411 SCV001198737 likely benign Marfan syndrome; Familial thoracic aortic aneurysm and aortic dissection 2023-08-28 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001183755 SCV001349574 uncertain significance Familial thoracic aortic aneurysm and aortic dissection 2023-02-28 criteria provided, single submitter clinical testing This missense variant replaces isoleucine with valine at codon 1948 of the FBN1 protein. Computational prediction suggests that this variant may not impact protein structure and function (internally defined REVEL score threshold <= 0.5, PMID: 27666373). To our knowledge, functional studies have not been performed for this variant. This variant has not been reported in individuals affected with cardiovascular disorders in the literature. This variant has been identified in 11/250900 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.
Fulgent Genetics, Fulgent Genetics RCV002497355 SCV002813295 uncertain significance Ectopia lentis 1, isolated, autosomal dominant; Marfan syndrome; MASS syndrome; Stiff skin syndrome; Weill-Marchesani syndrome 2, dominant; Acromicric dysplasia; Geleophysic dysplasia 2; Progeroid and marfanoid aspect-lipodystrophy syndrome 2021-10-02 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004004693 SCV004814626 uncertain significance Marfan syndrome 2023-05-04 criteria provided, single submitter clinical testing This missense variant replaces isoleucine with valine at codon 1948 of the FBN1 protein. Computational prediction suggests that this variant may not impact protein structure and function (internally defined REVEL score threshold <= 0.5, PMID: 27666373). To our knowledge, functional studies have not been performed for this variant. This variant has not been reported in individuals affected with cardiovascular disorders in the literature. This variant has been identified in 11/250900 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.

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