ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2165-19G>C

dbSNP: rs1555517632
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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 RCV000777333 SCV000913195 likely benign Hereditary cancer-predisposing syndrome 2018-01-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002535606 SCV003491714 likely benign Hereditary diffuse gastric adenocarcinoma 2022-04-17 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002535606 SCV005405211 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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