ClinVar Miner

Submissions for variant NM_017802.4(DNAAF5):c.1024+11G>T

dbSNP: rs201554395
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000250119 SCV000313006 benign not specified criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000515088 SCV000610619 likely benign not provided 2017-09-08 criteria provided, single submitter clinical testing
Invitae RCV002058273 SCV002406254 benign Primary ciliary dyskinesia 2024-01-12 criteria provided, single submitter clinical testing

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