ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1008+16G>C

dbSNP: rs780181188
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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 RCV001180109 SCV001344971 likely benign Hereditary cancer-predisposing syndrome 2018-12-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002068268 SCV002370167 likely benign Hereditary diffuse gastric adenocarcinoma 2023-11-24 criteria provided, single submitter clinical testing

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