ClinVar Miner

Submissions for variant NM_000203.5(IDUA):c.1402+36T>C (rs115134980)

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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 RCV000248587 SCV000302967 benign not specified criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001543884 SCV001762772 benign Hurler syndrome 2021-07-10 criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001543885 SCV001762773 benign Mucopolysaccharidosis, MPS-I-H/S 2021-07-10 criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001543886 SCV001762774 benign Mucopolysaccharidosis, MPS-I-S 2021-07-10 criteria provided, single submitter clinical testing
GeneDx RCV001618373 SCV001845151 benign not provided 2018-07-05 criteria provided, single submitter clinical testing

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