ClinVar Miner

Submissions for variant NM_001793.5(CDH3):c.-302C>T

gnomAD frequency: 0.00002  dbSNP: rs145687049
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000263804 SCV000398486 uncertain significance EEM syndrome 2016-06-14 criteria provided, single submitter clinical testing

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