ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.163+17G>A

gnomAD frequency: 0.00001  dbSNP: rs1005743424
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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 RCV000777141 SCV000912830 likely benign Hereditary cancer-predisposing syndrome 2017-12-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002535596 SCV003224741 likely benign Hereditary diffuse gastric adenocarcinoma 2023-10-18 criteria provided, single submitter clinical testing

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