ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1138-44G>A

gnomAD frequency: 0.00009  dbSNP: rs374676556
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000989623 SCV001140142 likely benign Hereditary diffuse gastric adenocarcinoma 2019-05-28 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268395 SCV002551765 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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