ClinVar Miner

Submissions for variant NM_012062.5(DNM1L):c.1885-15del

dbSNP: rs863223951
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000198062 SCV000251345 benign not specified 2014-03-31 criteria provided, single submitter clinical testing The variant is found in MITONUC-MITOP panel(s).
PreventionGenetics, part of Exact Sciences RCV000198062 SCV000311817 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001516215 SCV001724456 benign not provided 2024-01-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002492902 SCV002802299 likely benign Optic atrophy 5; Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1 2021-09-01 criteria provided, single submitter clinical testing

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