ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2268T>C (p.Asp756=)

dbSNP: rs1567515480
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000866766 SCV001007905 likely benign not provided 2015-12-20 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004789243 SCV005404157 benign Hereditary diffuse gastric adenocarcinoma 2024-09-23 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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