ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.49-8dup

dbSNP: rs1240151598
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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 RCV000581414 SCV000689551 likely benign Hereditary cancer-predisposing syndrome 2017-09-05 criteria provided, single submitter clinical testing
GeneDx RCV001672885 SCV001890383 benign not provided 2015-04-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061801 SCV002351806 benign Hereditary diffuse gastric adenocarcinoma 2024-01-05 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002061801 SCV005404253 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-11 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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