ClinVar Miner

Submissions for variant NM_000192.3(TBX5):c.663+36G>T (rs2236017)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000251038 SCV000302913 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000128533 SCV001944038 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Molecular Genetics and Enzymology, National Research Centre RCV000128533 SCV000172177 unknown not provided no assertion criteria provided not provided Converted during submission to Uncertain significance.

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