ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.48+12C>A

dbSNP: rs1221801902
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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 RCV000583155 SCV000689541 likely benign Hereditary cancer-predisposing syndrome 2017-06-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002529232 SCV003490068 likely benign Hereditary diffuse gastric adenocarcinoma 2023-08-07 criteria provided, single submitter clinical testing

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