ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.688-15A>T

dbSNP: rs1555515410
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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 RCV000581574 SCV000689560 likely benign Hereditary cancer-predisposing syndrome 2017-03-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003624423 SCV004480593 likely benign Hereditary diffuse gastric adenocarcinoma 2023-02-03 criteria provided, single submitter clinical testing

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