ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1321-11del

dbSNP: rs761117936
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002158551 SCV002465239 likely benign Hereditary diffuse gastric adenocarcinoma 2022-08-08 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV004596526 SCV005090243 likely benign not specified 2024-07-31 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002158551 SCV005407146 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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