ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.531+20G>A

gnomAD frequency: 0.00001  dbSNP: rs1960732460
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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 RCV001185120 SCV001351273 likely benign Hereditary cancer-predisposing syndrome 2019-04-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003512106 SCV004272006 likely benign Hereditary diffuse gastric adenocarcinoma 2023-02-09 criteria provided, single submitter clinical testing

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