ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.163+16C>T

dbSNP: rs1395024294
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000777352 SCV000913214 likely benign Hereditary cancer-predisposing syndrome 2018-01-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067356 SCV002344847 likely benign Hereditary diffuse gastric adenocarcinoma 2023-05-11 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV004596346 SCV005090235 likely benign not specified 2024-07-31 criteria provided, single submitter clinical testing

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