ClinVar Miner

Submissions for variant NM_005654.6(NR2F1):c.690C>T (p.Ala230=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002469499 SCV002765236 uncertain significance not provided 2022-12-12 criteria provided, single submitter clinical testing In silico analysis supports that this variant does not alter splicing; Has not been previously published as pathogenic or benign to our knowledge

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