ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1712-3T>C

dbSNP: rs1269786119
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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 RCV001176677 SCV001340717 uncertain significance Hereditary cancer-predisposing syndrome 2019-03-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001322475 SCV001513349 likely benign Hereditary diffuse gastric adenocarcinoma 2023-08-10 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001322475 SCV005404300 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-19 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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