ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.687+18G>A

dbSNP: rs544659881
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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 RCV000774765 SCV000908721 likely benign Hereditary cancer-predisposing syndrome 2018-06-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068517 SCV002438190 likely benign Hereditary diffuse gastric adenocarcinoma 2023-02-24 criteria provided, single submitter clinical testing

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