ClinVar Miner

Submissions for variant NM_004625.4(WNT7A):c.861G>A (p.Val287=)

gnomAD frequency: 0.00210  dbSNP: rs149962459
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000178217 SCV000230237 uncertain significance not provided 2014-10-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000178217 SCV001105515 benign not provided 2024-12-03 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003479046 SCV004222956 likely benign not specified 2023-11-20 criteria provided, single submitter clinical testing

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