ClinVar Miner

Submissions for variant NM_030753.5(WNT3):c.322+18del

gnomAD frequency: 0.00277  dbSNP: rs778923631
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000614235 SCV000727798 likely benign not specified 2018-02-16 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV002064320 SCV002403748 benign not provided 2024-01-25 criteria provided, single submitter clinical testing

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