ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.72G>A (p.Glu24=)

dbSNP: rs2152114363
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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 RCV001805244 SCV002052047 likely benign Hereditary cancer-predisposing syndrome 2021-07-13 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004785319 SCV005405302 benign Hereditary diffuse gastric adenocarcinoma 2024-09-11 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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