ClinVar Miner

Submissions for variant NM_003394.4(WNT10B):c.854T>C (p.Ile285Thr)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002961935 SCV003195145 uncertain significance not provided 2022-07-13 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Labcorp Genetics (formerly Invitae), Labcorp RCV002961935 SCV003280906 likely benign not provided 2025-01-08 criteria provided, single submitter clinical testing

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