ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1711+9G>A

gnomAD frequency: 0.00010  dbSNP: rs368770384
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001082470 SCV000253410 likely benign Hereditary diffuse gastric adenocarcinoma 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV000431343 SCV000515757 likely benign not specified 2017-07-17 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Color Diagnostics, LLC DBA Color Health RCV000581165 SCV000689485 likely benign Hereditary cancer-predisposing syndrome 2017-01-12 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000679564 SCV000806641 likely benign not provided 2017-07-14 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000679564 SCV001469487 benign not provided 2020-09-10 criteria provided, single submitter clinical testing

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