ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1026C>T (p.Thr342=)

dbSNP: rs2152132512
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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 RCV002133713 SCV002454191 likely benign Hereditary diffuse gastric adenocarcinoma 2021-08-27 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV003478946 SCV004220772 likely benign not provided 2023-05-26 criteria provided, single submitter clinical testing

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