ClinVar Miner

Submissions for variant NM_001793.6(CDH3):c.2364C>T (p.Asp788=)

gnomAD frequency: 0.00009  dbSNP: rs144637479
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000392878 SCV000344120 uncertain significance not provided 2016-08-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000392878 SCV001647065 likely benign not provided 2024-10-30 criteria provided, single submitter clinical testing

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