ClinVar Miner

Submissions for variant NM_000202.8(IDS):c.419-6del

dbSNP: rs781852261
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001515856 SCV001724018 benign Mucopolysaccharidosis, MPS-II 2024-01-25 criteria provided, single submitter clinical testing
GeneDx RCV000675882 SCV001787504 likely benign not provided 2019-09-26 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000675882 SCV000801608 uncertain significance not provided 2015-10-26 no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000675882 SCV001926011 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001726300 SCV001967236 benign not specified no assertion criteria provided clinical testing
Natera, Inc. RCV001830470 SCV002084492 benign Mucopolysaccharidosis, MPS-III-A 2019-09-09 no assertion criteria provided clinical testing

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