ClinVar Miner

Submissions for variant NM_018122.5(DARS2):c.228-20del

dbSNP: rs143246542
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 RCV000676386 SCV001802600 likely benign not provided 2019-08-13 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000676386 SCV000802162 benign not provided 2016-02-22 no assertion criteria provided clinical testing

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