ClinVar Miner

Submissions for variant NM_001330311.2(DVL1):c.1777C>T (p.Arg593Trp)

gnomAD frequency: 0.00014  dbSNP: rs372681220
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514751 SCV000609816 uncertain significance not provided 2017-08-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000514751 SCV002206041 benign not provided 2023-05-20 criteria provided, single submitter clinical testing

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