ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.688-11G>T

dbSNP: rs2152130974
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002084266 SCV002429240 likely benign Hereditary diffuse gastric adenocarcinoma 2022-09-01 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002084266 SCV005405304 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-13 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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