ClinVar Miner

Submissions for variant NM_000138.5(FBN1):c.69T>C (p.His23=)

dbSNP: rs2140787712
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago RCV002208741 SCV002495766 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 2021-03-19 criteria provided, single submitter clinical testing FBN1 NM_000138.4 exon 2 p.His23= (c.69T>C): This variant has not been reported in the literature and is not present in large control databases. Evolutionary conservation and computational predictive tools for this variant are limited or unavailable. Of note, this variant is a silent variant and does not change the amino acid, reducing the probability that this variant is disease causing. In summary, data on this variant is insufficient for disease classification. Therefore, the clinical significance of this variant is uncertain.
Labcorp Genetics (formerly Invitae), Labcorp RCV003089102 SCV003493925 likely benign Marfan syndrome; Familial thoracic aortic aneurysm and aortic dissection 2022-04-25 criteria provided, single submitter clinical testing

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