ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.833-9C>T

dbSNP: rs878854698
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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 RCV001185365 SCV001351560 likely benign Hereditary cancer-predisposing syndrome 2021-06-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067962 SCV002486412 likely benign Hereditary diffuse gastric adenocarcinoma 2023-07-12 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002067962 SCV005405956 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-16 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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