ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1937-9T>A

dbSNP: rs765700023
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002542321 SCV001082586 likely benign Hereditary diffuse gastric adenocarcinoma 2024-01-07 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001187272 SCV001354010 likely benign Hereditary cancer-predisposing syndrome 2018-05-01 criteria provided, single submitter clinical testing

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