ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1008+15G>A

dbSNP: rs1057520564
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000434800 SCV000516055 likely benign not specified 2016-07-06 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.
Color Diagnostics, LLC DBA Color Health RCV000579668 SCV000684320 likely benign Hereditary cancer-predisposing syndrome 2016-08-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061608 SCV002414749 likely benign Hereditary diffuse gastric adenocarcinoma 2022-08-20 criteria provided, single submitter clinical testing

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