ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.688-18del

dbSNP: rs1960778485
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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 RCV001176674 SCV001340714 likely benign Hereditary cancer-predisposing syndrome 2019-03-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067879 SCV002361915 likely benign Hereditary diffuse gastric adenocarcinoma 2023-11-27 criteria provided, single submitter clinical testing

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