ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2296-12T>C

dbSNP: rs1555517817
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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 RCV000580038 SCV000684418 uncertain significance Hereditary cancer-predisposing syndrome 2019-04-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002060552 SCV002382476 likely benign Hereditary diffuse gastric adenocarcinoma 2023-12-15 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002060552 SCV005405206 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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