ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.702T>C (p.Ala234=)

dbSNP: rs1555515428
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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 RCV002196212 SCV002492683 likely benign Hereditary diffuse gastric adenocarcinoma 2022-09-06 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003492740 SCV004240434 likely benign Breast and/or ovarian cancer 2023-03-07 criteria provided, single submitter clinical testing

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