ClinVar Miner

Submissions for variant NM_002700.3(POU4F3):c.770C>T (p.Ala257Val)

dbSNP: rs765036368
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Deafness Molecular Diagnostic Center, Chinese PLA General Hospital RCV001823217 SCV001763656 uncertain significance Autosomal dominant nonsyndromic hearing loss 15 no assertion criteria provided case-control

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