ClinVar Miner

Submissions for variant NM_001303052.2(MYT1L):c.1817+15T>G

gnomAD frequency: 0.00500  dbSNP: rs180992065
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Total submissions: 2
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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 RCV000513832 SCV000610611 likely benign not provided 2017-06-26 criteria provided, single submitter clinical testing
GeneDx RCV000513832 SCV001949748 benign not provided 2020-07-22 criteria provided, single submitter clinical testing

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