ClinVar Miner

Submissions for variant NM_004933.3(CDH15):c.1876C>T (p.Leu626Phe)

gnomAD frequency: 0.00536  dbSNP: rs78261372
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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 RCV000514969 SCV000609599 likely benign not provided 2017-05-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000514969 SCV001101961 benign not provided 2019-12-31 criteria provided, single submitter clinical testing

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