ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1152G>A (p.Val384=)

dbSNP: rs1960890121
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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 RCV001180449 SCV001345382 likely benign Hereditary cancer-predisposing syndrome 2019-06-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001432066 SCV001634830 likely benign Hereditary diffuse gastric adenocarcinoma 2021-04-30 criteria provided, single submitter clinical testing

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