ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1181C>A (p.Thr394Asn)

dbSNP: rs1332444039
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
St. Jude Molecular Pathology, St. Jude Children's Research Hospital RCV000761002 SCV000890917 uncertain significance Hereditary diffuse gastric adenocarcinoma 2020-09-11 criteria provided, single submitter clinical testing

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