ClinVar Miner

Submissions for variant NM_153700.2(STRC):c.3557_5328del (p.Gln1186fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
WangQJ Lab, Chinese People's Liberation Army General Hospital RCV001822917 SCV001762446 likely pathogenic Autosomal recessive nonsyndromic hearing loss 16 2021-07-01 no assertion criteria provided clinical testing

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