ClinVar Miner

Submissions for variant NM_001793.4(CDH3):c.-634_-633insG

gnomAD frequency: 0.00041  dbSNP: rs886052224
Minimum review status: Collection method:
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000314275 SCV000398481 uncertain significance EEM syndrome 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694285 SCV005193455 uncertain significance not provided criteria provided, single submitter not provided

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