ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1711+7G>T

gnomAD frequency: 0.00001  dbSNP: rs762005138
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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 RCV000457522 SCV000545445 likely benign Hereditary diffuse gastric adenocarcinoma 2023-08-30 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000583506 SCV000689484 likely benign Hereditary cancer-predisposing syndrome 2017-01-16 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000457522 SCV005405914 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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