ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2165-10A>C

gnomAD frequency: 0.00001  dbSNP: rs753982211
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000199867 SCV000254820 likely benign Hereditary diffuse gastric adenocarcinoma 2024-01-21 criteria provided, single submitter clinical testing
GeneDx RCV001722112 SCV000512528 likely benign not provided 2020-11-27 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000580756 SCV000684402 likely benign Hereditary cancer-predisposing syndrome 2016-02-22 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000199867 SCV005405271 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-20 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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