ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.48+105A>G

gnomAD frequency: 0.00371  dbSNP: rs62057828
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV004705040 SCV005219056 likely benign not provided criteria provided, single submitter not provided
University of Washington Department of Laboratory Medicine, University of Washington RCV000209553 SCV000265093 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing

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