ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2406C>T (p.Ala802=)

dbSNP: rs1555517903
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000507097 SCV000600978 likely benign not specified 2016-09-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001400434 SCV001602238 likely benign Hereditary diffuse gastric adenocarcinoma 2022-10-26 criteria provided, single submitter clinical testing

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