ClinVar Miner

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

dbSNP: rs2152138120
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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 RCV002082285 SCV002436345 likely benign Hereditary diffuse gastric adenocarcinoma 2024-05-18 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.
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005361973 SCV005916189 likely benign Familial cancer of breast; Ovarian cancer 2019-11-07 criteria provided, single submitter clinical testing

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