ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2439+18_2439+32del

dbSNP: rs1567516239
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001178908 SCV001343473 likely benign Hereditary cancer-predisposing syndrome 2018-12-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068229 SCV002458756 likely benign Hereditary diffuse gastric adenocarcinoma 2022-08-23 criteria provided, single submitter clinical testing

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