ClinVar Miner

Submissions for variant NM_001349.4(DARS1):c.301A>T (p.Met101Leu)

gnomAD frequency: 0.00008  dbSNP: rs138416697
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514286 SCV000610440 uncertain significance not provided 2017-05-19 criteria provided, single submitter clinical testing

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