ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1008+11_1008+19del

dbSNP: rs1567506816
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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 RCV000777583 SCV000913446 uncertain significance Hereditary cancer-predisposing syndrome 2019-04-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061119 SCV002397427 likely benign Hereditary diffuse gastric adenocarcinoma 2023-08-22 criteria provided, single submitter clinical testing

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