ClinVar Miner

Submissions for variant NM_012062.5(DNM1L):c.741-208G>C

gnomAD frequency: 0.03525  dbSNP: rs75684791
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001574100 SCV001800853 likely benign not provided 2018-06-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001574100 SCV005216577 likely benign not provided criteria provided, single submitter not provided

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