ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.388-7C>T

dbSNP: rs201402744
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000541667 SCV000637828 likely benign Hereditary diffuse gastric adenocarcinoma 2023-07-13 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000541667 SCV005404532 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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