ClinVar Miner

Submissions for variant NM_000203.5(IDUA):c.590-45G>C (rs6829789)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000241615 SCV000302980 benign not specified criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001543817 SCV001762687 benign Hurler syndrome 2021-07-10 criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001543818 SCV001762688 benign Mucopolysaccharidosis, MPS-I-H/S 2021-07-10 criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001543819 SCV001762689 benign Mucopolysaccharidosis, MPS-I-S 2021-07-10 criteria provided, single submitter clinical testing
GeneDx RCV001689782 SCV001910507 benign not provided 2018-07-05 criteria provided, single submitter clinical testing

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