ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.470T>C (p.Val157Ala)

dbSNP: rs587783046
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Pathway Genomics RCV000144589 SCV000189913 uncertain significance Hereditary diffuse gastric adenocarcinoma 2014-07-24 no assertion criteria provided clinical testing

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