ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.2070G>A (p.Gly690=)

dbSNP: rs757587966
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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 RCV000526872 SCV000637767 likely benign Hereditary diffuse gastric adenocarcinoma 2017-02-20 criteria provided, single submitter clinical testing

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