ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1138-15C>G

gnomAD frequency: 0.00001  dbSNP: rs752733398
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000663102 SCV000786213 likely benign Hereditary diffuse gastric adenocarcinoma 2018-03-22 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001187080 SCV001353744 likely benign Hereditary cancer-predisposing syndrome 2023-05-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000663102 SCV002398093 likely benign Hereditary diffuse gastric adenocarcinoma 2023-11-24 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000663102 SCV004019574 uncertain significance Hereditary diffuse gastric adenocarcinoma 2023-03-03 criteria provided, single submitter clinical testing This variant is classified as a variant of uncertain significance as there is insufficient evidence to determine its impact on protein function and/or cancer risk.

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