ClinVar Miner

Submissions for variant NM_018122.5(DARS2):c.128-6_128-5dup

dbSNP: rs746151025
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 RCV000676381 SCV002032715 likely benign not provided 2021-06-13 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000676381 SCV000802157 benign not provided 2016-03-16 no assertion criteria provided clinical testing

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