ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1712-14G>A

dbSNP: rs2152138120
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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 RCV002082285 SCV002436345 likely benign Hereditary diffuse gastric adenocarcinoma 2021-08-05 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003492736 SCV004240424 uncertain significance Breast and/or ovarian cancer 2022-12-23 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002082285 SCV005404215 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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