ClinVar Miner

Submissions for variant NM_000263.4(NAGLU):c.532-96A>G

gnomAD frequency: 0.14585  dbSNP: rs2676533
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001687431 SCV001902666 benign not provided 2018-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001687431 SCV005250411 benign not provided criteria provided, single submitter not provided

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