ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1770C>T (p.Asp590=)

dbSNP: rs864622319
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000582394 SCV000689486 likely benign Hereditary cancer-predisposing syndrome 2017-06-12 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004787996 SCV005405981 benign Hereditary diffuse gastric adenocarcinoma 2024-09-20 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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