ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1008+12G>A

dbSNP: rs756154578
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001190805 SCV001358389 likely benign Hereditary cancer-predisposing syndrome 2019-07-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002069131 SCV002467161 likely benign Hereditary diffuse gastric adenocarcinoma 2021-08-05 criteria provided, single submitter clinical testing

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