ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2440-18T>C

dbSNP: rs773215346
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000774778 SCV000908770 likely benign Hereditary cancer-predisposing syndrome 2017-09-05 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268277 SCV002551799 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003512078 SCV004275411 likely benign Hereditary diffuse gastric adenocarcinoma 2023-06-19 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV003512078 SCV005403905 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-23 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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