ClinVar Miner

Submissions for variant NM_198999.3(SLC26A5):c.1514+1G>A

dbSNP: rs727504481
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000155610 SCV000205318 not provided Nonsyndromic genetic hearing loss 2013-03-11 no assertion provided clinical testing

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