ClinVar Miner

Submissions for variant NM_001039141.3(TRIOBP):c.6324+46C>G

gnomAD frequency: 0.96820  dbSNP: rs5756810
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001597952 SCV001830239 benign not provided 2018-06-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838688 SCV002098777 benign Autosomal recessive nonsyndromic hearing loss 28 2021-09-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001597952 SCV005278659 benign not provided criteria provided, single submitter not provided

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