ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1009-16_1009-15del

dbSNP: rs1567506961
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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 RCV000777093 SCV000912777 likely benign Hereditary cancer-predisposing syndrome 2017-12-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067352 SCV002388921 likely benign Hereditary diffuse gastric adenocarcinoma 2023-02-14 criteria provided, single submitter clinical testing

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