ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1937-4C>T

dbSNP: rs1057523153
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000583263 SCV000689495 likely benign Hereditary cancer-predisposing syndrome 2017-10-02 criteria provided, single submitter clinical testing
Mendelics RCV000989625 SCV001140147 uncertain significance Hereditary diffuse gastric adenocarcinoma 2019-05-28 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316767 SCV004017028 likely benign Malignant tumor of prostate 2023-07-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000989625 SCV004658957 likely benign Hereditary diffuse gastric adenocarcinoma 2023-10-22 criteria provided, single submitter clinical testing

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