ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.387+18T>C

gnomAD frequency: 0.00001  dbSNP: rs751887336
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000583973 SCV000689533 likely benign Hereditary cancer-predisposing syndrome 2016-03-04 criteria provided, single submitter clinical testing
GeneDx RCV000602304 SCV000722970 likely benign not specified 2017-09-15 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV002061798 SCV002395558 likely benign Hereditary diffuse gastric adenocarcinoma 2024-01-31 criteria provided, single submitter clinical testing

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