ClinVar Miner

Submissions for variant NM_007118.4(TRIO):c.8047+17T>C

gnomAD frequency: 0.00932  dbSNP: rs80292429
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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 RCV000513672 SCV000609591 likely benign not provided 2017-04-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000513672 SCV005259699 likely benign not provided criteria provided, single submitter not provided

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