ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1936+12A>G

dbSNP: rs1555516903
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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 RCV000583913 SCV000689493 likely benign Hereditary cancer-predisposing syndrome 2017-05-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003512056 SCV004368196 likely benign Hereditary diffuse gastric adenocarcinoma 2023-12-23 criteria provided, single submitter clinical testing

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