ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1242C>T (p.Thr414=)

dbSNP: rs779601817
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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 RCV001442293 SCV001645242 likely benign Hereditary diffuse gastric adenocarcinoma 2023-12-29 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV003478834 SCV004220783 likely benign not provided 2022-12-06 criteria provided, single submitter clinical testing

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