ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1009-8C>T

gnomAD frequency: 0.00001  dbSNP: rs201227194
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001705555 SCV000512515 likely benign not provided 2018-09-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000465396 SCV000557422 likely benign Hereditary diffuse gastric adenocarcinoma 2024-01-11 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001179335 SCV001343976 likely benign Hereditary cancer-predisposing syndrome 2017-09-20 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000465396 SCV005402952 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-17 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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