ClinVar Miner

Submissions for variant NM_001793.6(CDH3):c.1704G>A (p.Thr568=)

gnomAD frequency: 0.00006  dbSNP: rs561193756
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000597821 SCV000709426 uncertain significance not provided 2017-06-28 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000597821 SCV001500085 likely benign not provided 2020-08-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000597821 SCV001731216 benign not provided 2023-12-19 criteria provided, single submitter clinical testing

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