ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1566-10C>G

dbSNP: rs778678297
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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 RCV001183938 SCV001349786 likely benign Hereditary cancer-predisposing syndrome 2020-03-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002559854 SCV003220469 likely benign Hereditary diffuse gastric adenocarcinoma 2022-07-11 criteria provided, single submitter clinical testing

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