ClinVar Miner

Submissions for variant NM_003392.7(WNT5A):c.6+18T>A

gnomAD frequency: 0.00004  dbSNP: rs192224802
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002091868 SCV002436086 likely benign not provided 2023-06-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500141 SCV002810678 likely benign Autosomal dominant Robinow syndrome 1 2021-08-26 criteria provided, single submitter clinical testing

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