ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1320+9G>T

dbSNP: rs1276697924
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002118858 SCV002448346 likely benign Hereditary diffuse gastric adenocarcinoma 2021-02-11 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002465926 SCV002760859 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002118858 SCV005404446 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-18 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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