ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.163+18G>A

dbSNP: rs1555509793
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000604088 SCV000717563 likely benign not specified 2017-03-23 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.
Labcorp Genetics (formerly Invitae), Labcorp RCV003767495 SCV004618073 likely benign Hereditary diffuse gastric adenocarcinoma 2023-12-31 criteria provided, single submitter clinical testing

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