ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1138-15C>T

dbSNP: rs752733398
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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 RCV000584281 SCV000689436 likely benign Hereditary cancer-predisposing syndrome 2017-11-06 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004787994 SCV005405701 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-18 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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