ClinVar Miner

Submissions for variant NM_016824.5(ADD3):c.2119TAAA[1] (p.Ter707=)

dbSNP: rs753541585
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514349 SCV000609838 uncertain significance not provided 2017-02-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000514349 SCV003279415 benign not provided 2023-08-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000514349 SCV005191022 uncertain significance not provided criteria provided, single submitter not provided

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