ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1137+20G>C

dbSNP: rs34210985
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000420069 SCV000512517 likely benign not specified 2016-11-01 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 RCV002521520 SCV003297625 likely benign Hereditary diffuse gastric adenocarcinoma 2022-10-04 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000420069 SCV005090240 likely benign not specified 2024-07-31 criteria provided, single submitter clinical testing

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