ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2296-18A>C

dbSNP: rs750381383
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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 RCV000584145 SCV000689510 likely benign Hereditary cancer-predisposing syndrome 2017-03-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061796 SCV002395298 likely benign Hereditary diffuse gastric adenocarcinoma 2024-01-02 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002061796 SCV005403913 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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