ClinVar Miner

Submissions for variant NM_001199107.2(TBC1D24):c.965+1G>A

dbSNP: rs1390045914
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
National Institute on Deafness and Communication Disorders, National Institutes of Health RCV001254817 SCV001430921 pathogenic Autosomal recessive nonsyndromic hearing loss 86 2020-07-10 no assertion criteria provided research

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