ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.1107C>A (p.Asn369Lys)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003147988 SCV003835504 uncertain significance Blepharocheilodontic syndrome 1 2022-10-12 criteria provided, single submitter clinical testing
Baylor Genetics RCV003147987 SCV003835818 uncertain significance Hereditary diffuse gastric adenocarcinoma 2022-10-12 criteria provided, single submitter clinical testing
Baylor Genetics RCV003147986 SCV003835889 uncertain significance Malignant tumor of prostate 2022-10-12 criteria provided, single submitter clinical testing

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