ClinVar Miner

Submissions for variant NM_018122.5(DARS2):c.228-10del

dbSNP: rs374122386
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000676390 SCV000564929 benign not provided 2019-01-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000676390 SCV002452045 benign not provided 2024-12-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV003343852 SCV004048872 benign Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome 2023-04-11 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000676390 SCV000802166 benign not provided 2017-06-30 no assertion criteria provided clinical testing

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