ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1566-9C>T

dbSNP: rs1555516509
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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 RCV000777556 SCV000913419 uncertain significance Hereditary cancer-predisposing syndrome 2019-04-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001469295 SCV001673374 likely benign Hereditary diffuse gastric adenocarcinoma 2022-05-18 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001469295 SCV005403081 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-19 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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