ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.833-19T>C

gnomAD frequency: 0.00001  dbSNP: rs762712874
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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 RCV000582285 SCV000689569 likely benign Hereditary cancer-predisposing syndrome 2017-03-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061803 SCV002420300 likely benign Hereditary diffuse gastric adenocarcinoma 2021-09-21 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002061803 SCV005406372 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-16 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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