ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.342C>T (p.Val114=)

dbSNP: rs1555514470
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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 RCV001180424 SCV001345352 likely benign Hereditary cancer-predisposing syndrome 2018-12-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003624446 SCV004384473 likely benign Hereditary diffuse gastric adenocarcinoma 2023-11-02 criteria provided, single submitter clinical testing

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