ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.164-20C>T

gnomAD frequency: 0.00001  dbSNP: rs751307555
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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 RCV000774759 SCV000908707 likely benign Hereditary cancer-predisposing syndrome 2017-11-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067307 SCV002371618 likely benign Hereditary diffuse gastric adenocarcinoma 2023-10-29 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002067307 SCV005405193 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-12 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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