ClinVar Miner

Submissions for variant NM_194248.3(OTOF):c.897+1G>T

dbSNP: rs483353049
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory; Baylor College of Medicine RCV000119821 SCV000154747 probable-pathogenic Autosomal recessive nonsyndromic hearing loss 9 criteria provided, single submitter not provided Converted during submission to Likely pathogenic.

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