ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.532-7T>C

gnomAD frequency: 0.00001  dbSNP: rs1432324307
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000582781 SCV000689555 likely benign Hereditary cancer-predisposing syndrome 2016-10-17 criteria provided, single submitter clinical testing
GeneDx RCV001696963 SCV000719670 likely benign not provided 2019-05-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001399743 SCV001601541 likely benign Hereditary diffuse gastric adenocarcinoma 2023-12-23 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001696963 SCV004220836 likely benign not provided 2023-01-18 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001399743 SCV005405299 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-13 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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