ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1062del (p.Gly354_Leu355insTer)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ RCV003330197 SCV004037215 pathogenic Hereditary diffuse gastric adenocarcinoma 2022-08-03 criteria provided, single submitter clinical testing
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ RCV003330198 SCV004037254 likely benign Spinocerebellar ataxia 45 2020-08-03 criteria provided, single submitter clinical testing
Baylor Genetics RCV003459837 SCV004215724 pathogenic Familial cancer of breast 2023-05-26 criteria provided, single submitter clinical testing

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