ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1116T>G (p.Pro372=)

dbSNP: rs1555515761
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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 RCV000582012 SCV000689434 likely benign Hereditary cancer-predisposing syndrome 2017-05-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000983632 SCV001131657 likely benign Hereditary diffuse gastric adenocarcinoma 2023-11-08 criteria provided, single submitter clinical testing

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