ClinVar Miner

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

dbSNP: rs143246542
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000676387 SCV000564927 likely benign not provided 2021-05-15 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 27408822)
Mayo Clinic Laboratories, Mayo Clinic RCV000676387 SCV000802163 benign not provided 2016-03-16 no assertion criteria provided clinical testing
GeneDx RCV000676387 SCV001857199 benign not provided 2019-08-15 flagged submission clinical testing

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