ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1566-10C>T

gnomAD frequency: 0.00001  dbSNP: rs778678297
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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 RCV001410861 SCV001612916 likely benign Hereditary diffuse gastric adenocarcinoma 2021-03-05 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV001410861 SCV005402774 likely benign Hereditary diffuse gastric adenocarcinoma 2024-09-19 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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