ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1722T>C (p.Val574=)

dbSNP: rs1961156325
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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 RCV002146551 SCV002468269 likely benign Hereditary diffuse gastric adenocarcinoma 2024-07-25 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002146551 SCV005405301 benign Hereditary diffuse gastric adenocarcinoma 2024-09-19 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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