ClinVar Miner

Submissions for variant NM_001378609.3(OTOGL):c.4279+1G>A

dbSNP: rs2137876491
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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 RCV001822957 SCV001762508 likely pathogenic Autosomal recessive nonsyndromic hearing loss 84B 2021-07-01 no assertion criteria provided clinical testing

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