ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.833-4C>A

dbSNP: rs1960833702
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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 RCV001185159 SCV001351313 uncertain significance Hereditary cancer-predisposing syndrome 2018-10-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067954 SCV002339130 likely benign Hereditary diffuse gastric adenocarcinoma 2022-03-21 criteria provided, single submitter clinical testing

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