ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.591T>G (p.Ala197=)

dbSNP: rs2152130151
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001439339 SCV001642224 likely benign Hereditary diffuse gastric adenocarcinoma 2020-08-24 criteria provided, single submitter clinical testing

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