ClinVar Miner

Submissions for variant NM_138691.3(TMC1):c.2218G>T (p.Glu740Ter)

dbSNP: rs1564583413
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery, Institute of Otolaryngology, Chinese PLA General Hospital RCV000770876 SCV000902390 pathogenic Autosomal recessive nonsyndromic hearing loss 7 2019-02-26 no assertion criteria provided case-control

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