ClinVar Miner

Submissions for variant NM_000090.4(COL3A1):c.*3C>A

dbSNP: rs1383823798
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001175880 SCV001339666 uncertain significance Familial thoracic aortic aneurysm and aortic dissection 2020-03-20 criteria provided, single submitter clinical testing This variant is located in the 3' untranslated region of the COL3A1 gene. Splice site prediction tools suggest that this variant may not impact RNA splicing. To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with cardiovascular disorders in the literature. This variant has not been identified 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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