ClinVar Miner

Submissions for variant NM_018122.5(DARS2):c.128-7_128-5dup

dbSNP: rs746151025
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000676379 SCV001777856 likely benign not provided 2020-01-24 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000676379 SCV000802155 benign not provided 2017-08-22 no assertion criteria provided clinical testing

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