ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.164-10T>C

dbSNP: rs1555514398
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000583985 SCV000689473 likely benign Hereditary cancer-predisposing syndrome 2017-09-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001400911 SCV001602722 likely benign Hereditary diffuse gastric adenocarcinoma 2022-07-22 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001400911 SCV005406469 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-12 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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