ClinVar Miner

Submissions for variant NM_000203.5(IDUA):c.612_615dup (p.Ser206fs)

dbSNP: rs875989947
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000211625 SCV000268689 pathogenic Hurler syndrome 2016-05-09 no assertion criteria provided clinical testing

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