ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1321-14T>C

dbSNP: rs1960956644
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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 RCV001179933 SCV001344736 likely benign Hereditary cancer-predisposing syndrome 2019-06-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067904 SCV002434865 likely benign Hereditary diffuse gastric adenocarcinoma 2023-06-20 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002067904 SCV005405153 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-18 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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