ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2295+16C>A

gnomAD frequency: 0.00001  dbSNP: rs778429713
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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 RCV000774775 SCV000908762 likely benign Hereditary cancer-predisposing syndrome 2018-04-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061096 SCV002359349 likely benign Hereditary diffuse gastric adenocarcinoma 2023-11-13 criteria provided, single submitter clinical testing

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