ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.531+16C>T

dbSNP: rs376565246
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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 RCV000583894 SCV000689553 likely benign Hereditary cancer-predisposing syndrome 2017-04-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061802 SCV002409331 likely benign Hereditary diffuse gastric adenocarcinoma 2024-01-20 criteria provided, single submitter clinical testing

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